Aryl and biaryl compounds having MCH modulatory activity

ABSTRACT

In one embodiment, this invention provides a novel class of compounds as antagonists of the MCH receptor, methods of preparing such compounds, pharmaceutical compositions containing one or more of the compounds, methods of preparing pharmaceutical formulations comprising one or more such compounds, and methods of treatment, prevention or amelioration or one or more of diseases associated with the MCH receptor. An illustrative inventive compound is shown below:

FIELD OF THE INVENTION

[0001] The present invention relates to antagonists formelanin-concentrating hormone (MCH) and their use in the treatment ofobesity, diabetes and related disorders. It generally discloses novelcompounds having MCH receptor modulatory activity, pharmaceuticalcompositions containing one or more such modulators, methods ofpreparing such modulators and methods of using such modulators to treatobesity, diabetes and related disorders. The invention specificallydiscloses certain novel aryl and biaryl compounds. This applicationclaims priority from U.S. provisional patent application, Serial No.60/277,534 filed Mar. 21, 2001.

BACKGROUND OF THE INVENTION

[0002] MCH, a 19-amino acid cyclic peptide, was first identified over adecade ago in teleost fish where it appears to regulate color change.More recently, MCH which is synthesized mainly in the lateralhypothalamus, a brain center regulating feeding behavior, has been thesubject of investigation for its possible role as a regulator of eatingbehavior in mammals. Central administration of MCH is known to stimulatefood intake and promote fat storage in rodents. It is also known thatmice that overexpress MCH are obese. As reported by Shimada et al.,Nature, Vol. 396 (Dec. 17, 1998), pp. 670-673, MCH-deficient mice havereduced body weight and leanness due to hypophagia (reduced feeding). Inview of their findings, the authors have suggested that antagonists ofMCH action may be effective for the treatment of obesity. U.S. Pat. No.5,908,830 discloses a combination therapy for the treatment of diabetesor obesity involving the administration of a metabolic rate increasingagent and a feeding behavior modifying agent, an example of the latterbeing an MCH antagonist. U.S. Pat. No. 6,043,246 discloses ureaderivatives said to be useful as neuropeptide Y receptor antagonists andas agents for the treatment of, inter alia, diseases of the metabolicsystem including obesity and diabetes. Published PCT patent applicationWO 00/27845 describes a class of compounds, characterized therein asspiroindolines, said to be selective neuropeptide Y Y5 antagonists anduseful for the treatment of obesity and the complications associatedtherewith. Commonly assigned, copending U.S. provisional patentapplication Serial No. 60/232,255, filed Sep. 14, 2000, discloses andclaims aryl-substituted urea neuropeptide Y Y5 antagonists and their usein the treatment of obesity, hyperphagia (increased feeding) anddiabetes.

[0003] GB-2304714A (Assignee: Sanofi) discloses piperidine derivativesof the formula:

[0004] where the various moieties are as defined.

[0005] FR 2717802-A1 discloses piperidines of the formula:

[0006] where the various moieties are as defined.

[0007] EP 428434-A discloses piperidines and piperazines of the formula:

[0008] where the various moieties are as defined.

[0009] EP 515240-A1 discloses compounds of the formula:

[0010] where the various moieties are as defined.

[0011] EP 559538-A1 discloses compounds of the formula:

[0012] where the various moieties are as defined.

[0013] EP 474561-A1 discloses compounds of the formula:

[0014] where the various moieties are as defined.

[0015] Copending patent application, Ser. No. ______,filed of even dateherewith, discloses certain novel compounds with MCH modulatoryactivity.

[0016] There is a need for new compounds, formulations, treatments andtherapies for MCH receptor modulation, diabetes and related disorders .It is, therefore, an object of this invention to provide compoundsuseful in the treatment or prevention or amelioration of such disorders.

[0017] A further object of the present invention is to provide methodsfor modulating the MCH receptor using the compounds and pharmaceuticalcompositions provided herein.

[0018] Another object herein is to provide methods of modulating MCHreceptors using the compounds provided herein.

SUMMARY OF THE INVENTION

[0019] In its many embodiments, the present invention provides a novelclass of compounds as antagonists of MCH receptor, methods of preparingsuch compounds, pharmaceutical compositions containing one or more suchcompounds, methods of preparing pharmaceutical formulations comprisingone or more such compounds, and methods of treatment, prevention oramelioration of one or more diseases associated with the MCH receptor.In one embodiment, the present application discloses a compound,including enantiomers, stereoisomers, rotamers, tautomers and prodrug ofsaid compound, and pharmaceutically acceptable salts or solvates of saidcompound or of said prodrug, said compound having the general structureshown in Formula I:

[0020] wherein:

[0021] Ar¹=unsubstituted or substituted phenyl, pyridine,pyridine-N-oxide, pyrazine or pyridazine, wherein the substituentsnumber from 0 to 5, may be the same or different and are independentlyselected from the group consisting of H, CN, OCF₃, F, Cl, Br, I, CONH₂,methylenedioxy, OR, CO₂H, CO₂R, and OH with R being a C₁-C₆ straightchain alkyl or branched alkyl or a C₃-C₇ cycloalkyl;

[0022] M is H or R;

[0023] Z=

[0024] where Ar² is an unsubstituted or substituted phenyl wherein thesubstituents number from 0 to 5, may be the same or different and areindependently selected from the group consisting F, Cl, Br, I, R, OR,N0₂, and CF₃;

[0025] n=0 to 6;

[0026] p=1-6;

[0027] R₁ may be the same or different and is independently selectedfrom the group consisting of R; NH₂; NHR; N(R)₂; N(R)₂→O; NH(CH₂)_(n)OR;N(R)SO₂R; NH(CH₂)_(n)—N(R)₂; N(R)SO₂(R);

[0028] where n is defined above and where Y is a moiety numbering 0 to 5which may be the same or different and are independently selected fromthe group consisting of H; OH; NH₂;

[0029] where n is defined above and t=1 to 5;

[0030] and R₂ is H or alkyl

[0031] The preferred representations for the various functionalities inFormula I are: For Ar¹: phenyl or pyridyl (more preferably 4-phenyl or4-pyridyl on the ring in Formula I), with one or more substituents onsaid phenyl or pyridyl independently selected from the group consistingof CN, OCF₃ and halogen, more preferably a phenyl with substituentsselected from CN, OCF₃, F and Cl, and still more preferably when atleast one of these preferred substituents is in position 3 or position 4on the ring with respect to said ring's attachment to the benzylicposition shown in Formula I.

[0032] For Z: Ar²—NH—CO, where Ar² is a phenyl which may optionally besubstituted with 1-5 moieties such as a halogen, OCH₃ or CF₃, morepreferably the substituent being F, Cl or OCH₃.

[0033] For R: preferably a C₁-C₄ straight chain or branched alkyl or aC₃-C₇ cycloalkyl.

[0034] For n: preferably 1-6, more preferably 2-4, and still morepreferably 2.

[0035] For M: H.

[0036] For R₁: preferably selected from the group consisting of NHR;N(R)₂; N(R)_(2→O; NH(CH) ₂)_(n)OCH₃; N(R)SO₂R; NH(CH₂)_(n)—N(R)₂;N(R)SO₂(R);

[0037] with the more preferable moieties being NHMe; NHEt; NMe₂;NH(CH₂)_(n)OCH₃; NH-cyclopropyl; NH-cyclobutyl; NH-cyclopentyl;NH(CH₂)₃NMe₂; and

[0038] where Y and n are as defined above.

[0039] For Y: preferably the moieties NH₂; NMe₂; NHMe;

[0040] The present invention also discloses a compound, includingenantiomers, stereoisomers, rotamers, tautomers and prodrug of saidcompound, and pharmaceutically acceptable salts or solvates of saidcompound or of said prodrug, said compound having the general structureshown in Formula II:

[0041] where M, Z, n, p and R₁ are defined above along with theirpreferences; k is a number from 0 to 5. X may be the same or different,and is independently selected from the group consisting of:

[0042] H, Cl, F, Br, I, R, OR, CF₃, OCF₃, methylenedioxy,

[0043] with the preferred moieties for X being R, H, Cl, CF₃ and OCF₃.The number k is preferably 1-3.

[0044] The present invention additionally discloses a compound,including enantiomers, stereoisomers, rotamers, tautomers and prodrug ofsaid compound, and pharmaceutically acceptable salts or solvates of saidcompound or of said prodrug, said compound having the general structureshown in Formula III:

[0045] where M, n, p and R₁ are defined above along with theirpreferences. R₂ is H or alkyl and k is a number 0 to 5. G is —CH₂—,—C(O)— or —C(O)—O— with the —C(O) linked to the N(R₁R₂) in the figure.R₃ is an alkyl, aryl, arylalkyl or alkylaryl. L may be the same ordifferent and is independently selected from the group consisting of H,aryl, alkyl, halogen, alkoxy, aryloxy, arylalkoxy, alkylaryloxy,hydroxy, carboxy, carboalkoxy, cyano, CF₃ and NO₂.

[0046] The ring moieties in the inventive compounds may optionally carrysubstituents or additional substituents on the ring. Such substituentsmay be, for example, R, halogen, alkoxy, aryloxy, arylalkoxy,alkylaryloxy, hydroxy, carboxy, carboalkoxy, cyano, trifluoroalkyl,nitro and the like.

[0047] Also included in the invention are tautomers, rotamers,enantiomers and other optical isomers of compounds of Formula I, FormulaII and Formula III where applicable, pharmaceutically acceptable salts,solvates and derivatives thereof, as well as prodrug of said compounds,and pharmaceutically acceptable salts, solvates and derivatives of saidprodrug.

[0048] A further feature of the invention is pharmaceutical compositionscontaining as active ingredient a compound of Formula I, Formula II orFormula III (or its salt, solvate or isomers) together with apharmaceutically acceptable carrier or excipient.

[0049] The invention also provides methods for preparing compounds ofFormula I, Formula II and Formula III, as well as methods for treatingdiseases such as, for example, obesity and related disorders. Themethods for treating comprise administering to a patient suffering fromsaid disease or diseases therapeutically effective amounts of a compoundof Formula I, Formula II or Formula III, or of pharmaceuticalcompositions comprising a compound of Formula I, Formula II or FormulaIII. The term “Therapeutically effective amounts” refers to amounts ofthe compound that are effective to make the compound function as MCHmodulator.

[0050] Also disclosed is the use of a compound of Formula I, Formula IIor of Formula III for the manufacture of a medicament for treatingobesity and related disorders.

[0051] In addition to monotherapies including the compound representedby Formula I, Formula II or Formula III, another aspect of thisinvention is combinations (such as, for example, dual combinationtherapy, three combination therapy and the like,) of therapeuticallyeffective amounts of a compound of Formula I (or Formula II or FormulaIII), or a prodrug thereof, or a pharmaceutically acceptable salt ofsaid compound or a pharmaceutically acceptable salt of said prodrug, andtherapeutically effective amounts of one or more antiobesity/anorecticagent such as, for example, a β₃ agonist, a thyromimetic agent, or anNPY antagonist.

[0052] Still another aspect of this invention is a method for treatingobesity comprising administering to a mammal (which term includeshumans) in need of such treatment:

[0053] a. therapeutically effective amounts of a first compound, saidfirst compound being a Formula I compound (or a Formula II compound or aFormula III compound), a prodrug thereof, or a pharmaceuticallyacceptable salt of said compound or a pharmaceutically acceptable saltof said prodrug; and

[0054] b. therapeutically effective amounts of a second compound, saidsecond compound being an antiobesity and/or anorectic agent such as, forexample, a β₃ agonist, a thyromimetic agent, or an NPY antagonist,wherein the amounts of the first and second compounds result in thedesired therapeutic effect of treating obesity.

[0055] This invention is also directed to a pharmaceutical compositioncomprising a combination of therapeutically effective amounts of a firstcompound, said first compound being a Formula I compound (or a FormulaII compound or a Formula III compound), a prodrug thereof, or apharmaceutically acceptable salt of said compound or a pharmaceuticallyacceptable salt of said prodrug; and therapeutically effective amountsof a second compound, said second compound being an antiobesity and/oranorectic agent such as, for example, a β₃ agonist, a thyromimeticagent, or an NPY antagonist; and/or optionally a pharmaceuticalacceptable carrier, vehicle or diluent.

[0056] Another aspect of this invention is a kit comprising:

[0057] a. therapeutically effective amounts of a first compound, saidfirst compound being a Formula I compound (or a Formula II compound or aFormula III compound), a prodrug thereof, or a pharmaceuticallyacceptable salt of said compound or a pharmaceutically acceptable saltof said prodrug; and a pharmaceutically acceptable carrier, vehicle ordiluent in a first unit dosage form;

[0058] b. therapeutically effective amounts of a second compound, saidsecond compound being an antiobesity and/or anorectic agent such as, forexample, a β₃ agonist, a thyromimetic agent, or an NPY antagonist; and apharmaceutically acceptable carrier, vehicle or diluent in a second unitdosage form; and

[0059] C. means for containing said first unit dosage form and saidsecond unit dosage form, wherein the amounts of the first compound andof the second compound result in the desired therapeutic effect oftreating obesity.

[0060] Illustrative non-limiting examples of preferred antiobesityand/or anorectic agents in the above combination methods, combinationcompositions and combination kits include: phenylpropanolamine,ephedrine, pseudoephedrine, phentermine, a cholecystokinin-A(hereinafter referred to as CCK-A) agonist, a monoamine reuptakeinhibitor (such as, for example, sibutramine), a sympathomimetic agent,a serotonergic agent (such as, for example, dexfenfluramine orfenfluramine), a dopamine agonist (such as, for example, bromocriptine),a melanocyte-stimulating hormone receptor agonist or mimetic, amelanocyte-stimulating hormone analog, a cannabinoid receptorantagonist, a melanin concentrating hormone antagonist, the OB protein(hereinafter referred to as “leptin”), a leptin analog, a leptinreceptor agonist, a galanin antagonist or a GI lipase inhibitor ordecreaser (such as orlistat). Other anorectic agents include bombesinagonists, dehydroepiandrosterone or analogs thereof, glucocorticoidreceptor agonists and antagonists, orexin receptor antagonists,urocortin binding protein antagonists, agonists of the glucagon-likepeptide-1 receptor such as, for example, Exendin and ciliaryneurotrophic factors such as, for example, Axokine.

[0061] Another aspect of this invention is a method for treatingdiabetes comprising administering to a mammal:

[0062] a. therapeutically effective amounts of a first compound, saidfirst compound being a Formula I compound (or a Formula II compound or aFormula III compound), a prodrug thereof, or a pharmaceuticallyacceptable salt of said compound or a pharmaceutically acceptable saltof said prodrug; and

[0063] b. therapeutically effective amounts of a second compound, saidsecond compound being an aldose reductase inhibitor, a glycogenphosphorylase inhibitor, a sorbitol dehydrogenase inhibitor, a proteintyrosine phosphatase 1B inhibitor, a dipeptidyl protease inhibitor,insulin (including orally bioavailable insulin preparations), an insulinmimetic, metformin, acarbose, a PPAR-gamma ligand such as troglitazone,rosaglitazone, pioglitazone or GW-1929, a sulfonylurea, glipazide,glyburide, or chlorpropamide wherein the amounts of the first and secondcompounds result in the therapeutic effect of treating diabetes.

[0064] This invention is also directed to a pharmaceutical compositioncomprising a combination of therapeutically effective amounts of a firstcompound, said first compound being a Formula I compound (or a FormulaII compound or a Formula III compound), a prodrug thereof, or apharmaceutically acceptable salt of said compound or a pharmaceuticallyacceptable salt of said prodrug; therapeutically effective amounts of asecond compound, said second compound being an aldose reductaseinhibitor, a glycogen phosphorylase inhibitor, a sorbitol dehydrogenaseinhibitor, a protein tyrosine phosphatase 1B inhibitor, a dipeptidylprotease inhibitor, insulin (including orally bioavailable insulinpreparations), an insulin mimetic, metformin, acarbose, a PPAR-gammaligand such as troglitazone, rosaglitazone, pioglitazone, or GW-1929, asulfonylurea, glipazide, glyburide, or chlorpropamide; and optionally

[0065] a pharmaceutically acceptable carrier, vehicle or diluent.

[0066] Another aspect of this invention is a kit comprising:

[0067] a. therapeutically effective amounts of a first compound, saidfirst compound being a Formula I compound (or a Formula II compound or aFormula III compound), a prodrug thereof, or a pharmaceuticallyacceptable salt of said compound or a pharmaceutically acceptable saltof said prodrug; and a pharmaceutically acceptable carrier, vehicle ordiluent in a first unit dosage form;

[0068] b. therapeutically effective amounts of an aldose reductaseinhibitor, a glycogen phosphorylase inhibitor, a sorbitol dehydrogenaseinhibitor, a protein tyrosine phosphatase 1B inhibitor, a dipeptidylprotease inhibitor, insulin (including orally bioavailable insulinpreparations), an insulin mimetic, metformin, acarbose, a PPAR-gammaligand such as troglitazone, rosaglitazone, pioglitazone, or GW-1929, asulfonylurea, glipazide, glyburide, or chlorpropamide; and apharmaceutically acceptable carrier, vehicle or diluent in a second unitdosage form; and

[0069] C. means for containing said first unit dosage form and saidsecond unit dosage form, wherein the amounts of the first compound andof the second compound result in the desired therapeutic effect oftreating diabetes.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

[0070] In one embodiment, the present invention discloses compounds ofFormula I, Formula II or Formula III, or a pharmaceutically acceptablederivative thereof, as inhibitors of MCH receptor. The variousdefinitions for the moieties in Formulas I, II and III are given above.

[0071] Unless defined otherwise, all technical and scientific terms usedherein have the same meaning as is commonly understood by one of skillin the art to which this invention belongs. Thus, for example, the termalkyl (including the alkyl portions of alkoxy) refers to a monovalentgroup derived from a straight or branched chain saturated hydrocarbon bythe removal of a single atom having from 1 to 8 carbon atoms, preferablyfrom 1 to 6;

[0072] aryl—represents a carbocyclic group having from 6 to 14 carbonatoms and having at least one benzenoid ring, with all availablesubstitutable aromatic carbon atoms of the carbocyclic group beingintended as possible points of attachment. Preferred aryl groups includephenyl, 1-naphthyl, 2-naphthyl and indanyl, and especially phenyl andsubstituted phenyl;

[0073] aralkyl—represents a moiety containing an aryl group linked viala lower alkyl;

[0074] alkylaryl—represents a moiety containing a lower alkyl linked viaan aryl group;

[0075] cycloalkyl—represents a saturated carbocyclic ring having from 3to 8 carbon atoms, preferably 5 or 6, optionally substituted.

[0076] heterocyclic—represents, in addition to the heteroaryl groupsdefined below, saturated and unsaturated cyclic organic groups having atleast one 0, S and/or N atom interrupting a carbocyclic ring structurethat consists of one ring or two fused rings, wherein each ring is 5-,6- or 7-membered and may or may not have double bonds that lackdelocalized pi electrons, which ring structure has from 2 to 8,preferably from 3 to 6 carbon atoms, e.g., 2- or 3-piperidinyl, 2- or3-piperazinyl, 2- or 3-morpholinyl, or 2- or 3-thiomorpholinyl;

[0077] halogen—represents fluorine, chlorine, bromine and iodine;

[0078] heteroaryl—represents a cyclic organic group having at least one0, S and/or N atom interrupting a carbocyclic ring structure and havinga sufficient number of delocalized pi electrons to provide aromaticcharacter, with the aromatic heterocyclyl group having from 2 to 14,preferably 4 or 5 carbon atoms, e.g., 2-, 3- or 4-pyridyl, 2- or3-furyl, 2- or 3-thienyl, 2-, 4- or 5-thiazolyl, 2- or 4-imidazolyl, 2-,4- or 5-pyrimidinyl, 2-pyrazinyl, or 3- or 4-pyridazinyl, etc.

[0079] Representative compounds of the invention which exhibit excellentMCH receptor modulatory activity are listed in Table I along with theiractivity (ranges of K_(i) values in nanomolar, nM).

[0080] Depending upon the structure, the compounds of the invention mayform pharmaceutically acceptable salts with organic or inorganic acids,or organic or inorganic bases. Examples of suitable acids for such saltformation are hydrochloric, sulfuric, phosphoric, acetic, citric,oxalic, malonic, salicylic, malic, fumaric, succinic, ascorbic, maleic,methanesulfonic and other mineral and carboxylic acids well known tothose skilled in the art. For formation of salts with bases, suitablebases are, for example, NaOH, KOH, NH₄OH, tetraalkylammonium hydroxide,and the like.

[0081] In another embodiment, this invention provides pharmaceuticalcompositions comprising the above-described inventive aryl or biarylcompounds as an active ingredient. The pharmaceutical compositionsgenerally additionally comprise a pharmaceutically acceptable carrierdiluent, excipient or carrier (collectively referred to herein ascarrier materials). Because of their MCH inhibitory activity, suchpharmaceutical compositions possess utility in treating obesity andrelated disorders.

[0082] In yet another embodiment, the present invention disclosesmethods for preparing pharmaceutical compositions comprising theinventive aryl or biaryl compounds as an active ingredient. In thepharmaceutical compositions and methods of the present invention, theactive ingredients will typically be administered in admixture withsuitable carrier materials suitably selected with respect to theintended form of administration, i.e. oral tablets, capsules (eithersolid-filled, semisolid filled or liquid filled), powders forconstitution, oral gels, elixirs, dispersible granules, syrups,suspensions, and the like, and consistent with conventionalpharmaceutical practices. For example, for oral administration in theform of tablets or capsules, the active drug component may be combinedwith any oral non-toxic pharmaceutically acceptable inert carrier, suchas lactose, starch, sucrose, cellulose, magnesium stearate, dicalciumphosphate, calcium sulfate, talc, mannitol, ethyl alcohol (liquid forms)and the like. Moreover, when desired or needed, suitable binders,lubricants, disintegrating agents and coloring agents may also beincorporated in the mixture. Powders and tablets may be comprised offrom about 5 to about 95 percent inventive composition. Suitable bindersinclude starch, gelatin, natural sugars, corn sweeteners, natural andsynthetic gums such as acacia, sodium alginate, carboxymethylcellulose,polyethylene glycol and waxes. Among the lubricants there may bementioned for use in these dosage forms, boric acid, sodium benzoate,sodium acetate, sodium chloride, and the like. Disintegrants includestarch, methylcellulose, guar gum and the like. Sweetening and flavoringagents and preservatives may also be included where appropriate. Some ofthe terms noted above, namely disintegrants, diluents, lubricants,binders and the like, are discussed in more detail below.

[0083] Additionally, the compositions of the present invention may beformulated in sustained release form to provide the rate controlledrelease of any one or more of the components or active ingredients tooptimize the therapeutic effects, i.e. MCH inhibitory activity and thelike. Suitable dosage forms for sustained release include layeredtablets containing layers of varying disintegration rates or controlledrelease polymeric matrices impregnated with the active components andshaped in tablet form or capsules containing such impregnated orencapsulated porous polymeric matrices.

[0084] Liquid form preparations include solutions, suspensions andemulsions. As an example may be mentioned water or water-propyleneglycol solutions for parenteral injections or addition of sweeteners andpacifiers for oral solutions, suspensions and emulsions. Liquid formpreparations may also include solutions for intranasal administration.

[0085] Aerosol preparations suitable for inhalation may includesolutions and solids in powder form, which may be in combination with apharmaceutically acceptable carrier such as inert compressed gas, e.g.nitrogen.

[0086] For preparing suppositories, a low melting wax such as a mixtureof fatty acid glycerides such as cocoa butter is first melted, and theactive ingredient is dispersed homogeneously therein by stirring orsimilar mixing. The molten homogeneous mixture is then poured intoconvenient sized molds, allowed to cool and thereby solidify.

[0087] Also included are solid form preparations which are intended tobe converted, shortly before use, to liquid form preparations for eitheroral or parenteral administration. Such liquid forms include solutions,suspensions and emulsions.

[0088] The compounds of the invention may also be deliverabletransdermally. The transdermal compositions may take the form of creams,lotions, aerosols and/or emulsions and can be included in a transdermalpatch of the matrix or reservoir type as are conventional in the art forthis purpose.

[0089] The compounds as well as the pharmaceutical formulationscontaining the inventive compounds may also be delivered subcutaneously.

[0090] Preferably the compound is administered orally.

[0091] Preferably, the pharmaceutical preparation is in a unit dosageform. In such form, the preparation is subdivided into suitably sizedunit doses containing appropriate quantities of the active components,e.g., an effective amount to achieve the desired purpose.

[0092] The quantity of the inventive active composition in a unit doseof preparation may be generally varied or adjusted from about 1.0milligram to about 1,000 milligrams, preferably from about 1.0 to about950 milligrams, more preferably from about 1.0 to about 500 milligrams,and typically from about 1 to about 250 milligrams, according to theparticular application. The actual dosage employed may be varieddepending upon the patient's age, sex, weight and severity of thecondition being treated. Such techniques are well known to those skilledin the art.

[0093] Generally, the human oral dosage form containing the activeingredients can be administered 1 or 2 times per day. The amount andfrequency of the administration will be regulated according to thejudgment of the attending clinician. A generally recommended dailydosage regimen for oral administration may range from about 1.0milligram to about 1,000 milligrams per day, in single or divided doses.

[0094] Some useful terms are described below:

[0095] Capsule—refers to a special container or enclosure made of methylcellulose, polyvinyl alcohols, or denatured gelatins or starch forholding or containing compositions comprising the active ingredients.Hard shell capsules are typically made of blends of relatively high gelstrength bone and pork skin gelatins. The capsule itself may containsmall amounts of dyes, opaquing agents, plasticizers and preservatives.

[0096] Tablet—refers to a compressed or molded solid dosage formcontaining the active ingredients with suitable diluents. The tablet canbe prepared by compression of mixtures or granulations obtained by wetgranulation, dry granulation or by compaction.

[0097] Oral gel—refers to the active ingredients dispersed orsolubilized in a hydrophillic semi-solid matrix.

[0098] Powder for constitution refers to powder blends containing theactive ingredients and suitable diluents which can be suspended in wateror juices.

[0099] Diluent—refers to substances that usually make up the majorportion of the composition or dosage form. Suitable diluents includesugars such as lactose, sucrose, mannitol and sorbitol; starches derivedfrom wheat, corn, rice and potato; and celluloses such asmicrocrystalline cellulose. The amount of diluent in the composition canrange from about 10 to about 90% by weight of the total composition,preferably from about 25 to about 75%, more preferably from about 30 toabout 60% by weight, even more preferably from about 12 to about 60%.

[0100] Disintegrant—refers to materials added to the composition to helpit break apart (disintegrate) and release the medicaments. Suitabledisintegrants include starches; “cold water soluble” modified starchessuch as sodium carboxymethyl starch; natural and synthetic gums such aslocust bean, karaya, guar, tragacanth and agar; cellulose derivativessuch as methylcellulose and sodium carboxymethylcellulose;microcrystalline celluloses and cross-linked microcrystalline cellulosessuch as sodium croscarmellose; alginates such as alginic acid and sodiumalginate; clays such as bentonites; and effervescent mixtures. Theamount of disintegrant in the composition can range from about 2 toabout 15% by weight of the composition, more preferably from about 4 toabout 10% by weight.

[0101] Binder—refers to substances that bind or “glue” powders togetherand make them cohesive by forming granules, thus serving as the“adhesive” in the formulation. Binders add cohesive strength alreadyavailable in the diluent or bulking agent. Suitable binders includesugars such as sucrose; starches derived from wheat, corn rice andpotato; natural gums such as acacia, gelatin and tragacanth; derivativesof seaweed such as alginic acid, sodium alginate and ammonium calciumalginate; cellulosic materials such as methylcellulose and sodiumcarboxymethylcellulose and hydroxypropylmethylcellulose;polyvinylpyrrolidone; and inorganics such as magnesium aluminumsilicate. The amount of binder in the composition can range from about 2to about 20% by weight of the composition, more preferably from about 3to about 10% by weight, even more preferably from about 3 to about 6% byweight.

[0102] Lubricant—refers to a substance added to the dosage form toenable the tablet, granules, etc. after it has been compressed, torelease from the mold or die by reducing friction or wear. Suitablelubricants include metallic stearates such as magnesium stearate,calcium stearate or potassium stearate; stearic acid; high melting pointwaxes; and water soluble lubricants such as sodium chloride, sodiumbenzoate, sodium acetate, sodium oleate, polyethylene glycols andd'l-leucine. Lubricants are usually added at the very last step beforecompression, since they must be present on the surfaces of the granulesand in between them and the parts of the tablet press. The amount oflubricant in the composition can range from about 0.2 to about 5% byweight of the composition, preferably from about 0.5 to about 2%, morepreferably from about 0.3 to about 1.5% by weight.

[0103] Glident—material that prevents caking and improve the flowcharacteristics of granulations, so that flow is smooth and uniform.Suitable glidents include silicon dioxide and talc. The amount ofglident in the composition can range from about 0.1% to about 5% byweight of the total composition, preferably from about 0.5 to about 2%by weight.

[0104] Coloring agents—excipients that provide coloration to thecomposition or the dosage form. Such excipients can include food gradedyes and food grade dyes adsorbed onto a suitable adsorbent such as clayor aluminum oxide. The amount of the coloring agent can vary from about0.1 to about 5% by weight of the composition, preferably from about 0.1to about 1%.

[0105] Bioavailability—refers to the rate and extent to which the activedrug ingredient or therapeutic moiety is absorbed into the systemiccirculation from an administered dosage form as compared to a standardor control.

[0106] Conventional methods for preparing tablets are known. Suchmethods include dry methods such as direct compression and compressionof granulation produced by compaction, or wet methods or other specialprocedures. Conventional methods for making other forms foradministration such as, for example, capsules, suppositories and thelike are also well known.

[0107] Another embodiment of the invention discloses the use of thepharmaceutical compositions disclosed above for treatment of diseasessuch as, for example, obesity and the like. The method comprisesadministering a therapeutically effective amount of the inventivepharmaceutical composition to a patient having such a disease ordiseases and in need of such a treatment.

[0108] As stated earlier, the invention also includes tautomers,enantiomers and other stereoisomers of the compounds where applicable.Thus, as one skilled in the art knows, some of the inventive compoundsmay exist in isomeric forms. Such variations are contemplated to bewithin the scope of the invention.

[0109] Another embodiment of the invention discloses a method of makingthe inventive aryl or biaryl compounds disclosed herein. The compoundsmay be prepared by several techniques known in the art. Representativeillustrative procedures are outlined in the following reaction schemes.

REACTION SCHEMES

[0110] Abbreviations which are used in the descriptions of the schemes,preparations and the examples that follow are:

[0111] Abbreviation used:

[0112] Ar=argon

[0113] Boc=tert-butyloxycarbonyl

[0114] tBuOH=tert-butanol

[0115] CH₂Cl₂=dichloromethane

[0116] CICH₂CH₂Cl=1,2-dichloroethane

[0117] CDI=carbonyldiimidazole

[0118] DIC=1,3-dicyclohexylcarbodiimide

[0119] DMF=N,N-dimethylformamide

[0120] DIEA=N,N-diisopropylethylamine

[0121] Et=ethyl

[0122] EtOH=ethanol

[0123] EtOAc=ethyl acetate

[0124] HOBt=1-hydroxybenzotriazole

[0125] H₂SO₄=sulfuric acid

[0126] HCl=hydrogen chloride

[0127] H₂O=water

[0128] K₂CO₃=potassium carbonate

[0129] LDA=lithium diisopropylamide

[0130] LiOH=lithium hydroxide

[0131] LiAlH₄=lithium aluminum hydride

[0132] Me=methyl

[0133] Mel=methyl iodide

[0134] MeOH=methanol

[0135] Me₂S=dimethylsulfide

[0136] NMMO=4-methylmorpholine N-oxide

[0137] Na(OAc)₃BH=sodium triacetoxyborohydride

[0138] NaCl=sodium chloride

[0139] NaH=sodium hydride

[0140] NaHCO₃=sodium bicarbonate

[0141] NaIO₄=sodium periodate

[0142] Na₂CO₃=sodium carbonate

[0143] NaOH=sodium hydroxide

[0144] Na₂SO₄=sodium sulfate

[0145] Na₂S₂O₃=sodium thiosulfate

[0146] O₃=ozone

[0147] O₂=oxygen

[0148] OsO₄=osmium tetroxide

[0149] Pd(PPh₃)₄=tetrakis(triphenylphosphine)palladium(O)

[0150] SOCl₂=thionyl chloride

[0151] TEA=triethylamine

[0152] TFA=trifluoroacetic acid

[0153] TMSOTf=trimethylsilyl trifluoromethanesulfonate

[0154] THF=tetrahydrofuran

[0155] HMCHR—CHO=membranes prepared from Chinese hamster ovary cellsthat overexpress human melanin concentrating hormone.

[0156] WGA-SPA beads=Scintillation Assay beads labeled with wheat germagglutinin

[0157] BSA=bovine serum albumin

[0158] MCH=melanin concentrating hormone

[0159] MCHR=melanin concentrating hormone receptor

[0160] Several methods for preparing the compounds of this invention andintermediates thereof are illustrated in the following reaction schemes.Starting materials are made using known procedures or as illustrated.

[0161] Reaction Schemes 1-2 may be used to synthesize reactionintermediates wherein the structures are aryl amines and aryl carboxylicacids. The synthetic methods used here are modified from knownliterature procedures, such as: (1) E. D. Edstrom and T. Livinghouse, J.Am. Chem. Soc. (1986), 1334-6; (2) C. P. Forbes and G. L. Wenteler, J.Chem. Soc., Chem. Comm., (1986), 279-80; and (3) S. Kano et al., Chem.Pharm. Bull., 1985, 33, 340-6.

[0162] In reaction Scheme 1, allylation of the arylacetonitrile may beaccomplished using LDA to generate an anion followed by coupling withallyl iodide. The resulting 4-cyano-4-aryl-but-1-ene may be converted toan amine by reduction of the nitrile group by treatment with LiAIH₄ toform 5-amino-4-aryl-but-1-ene. Alternatively, the4-cyano-4-aryl-but-1-ene may be further alkylated, as illustrated usingLDA and Mel, to form 4-cyano-4-aryl-4-alkyl-but-1-ene. Reduction of thenitrile group using LiAlH₄ affords 5-amino-4-aryl-4-alkyl-but-1-ene.

[0163] In reaction Scheme 2, a commercially available aryl acetic acidis first converted to a methyl ester using MeOH/HCI(g). The methyl estermay be allylated using LDA and allyl iodide to form 2-arylpent-4-enoicacid methyl ester. The ester group may be hydrolyzed using a suitablebase, such as LiOH in THF/H₂O, to form the carboxylic acid, which can befurther converted to the acid chloride using SOCl₂. Alternatively, the2-aryl-pent-4-enoic acid methyl ester may be further alkylated, asillustrated using LDA and Mel, to form 2-aryl-2-alkylpent-4-enoic acidmethyl ester. The ester may be then hydrolyzed using a suitable base,such as LiOH in THF/H₂O, to form the corresponding carboxylic acidintermediate, which can be converted to the acid chloride using SOCl₂.

[0164] Scheme 3 outlines a general method for preparing compounds ofFormula I of the invention using a novel solid phase synthesis method.The synthesis begins with the coupling of a suitable linker, asillustrated using an acid cleavable linker4-(4-formyl-3-methoxy-phenoxy)-butyric acid, to a suitable amino resinthrough amide bond formation. Reductive amination of the linker aldehydewith the amine synthon 5-amino-4-aryl-4-R-but-1-ene forms a secondaryamine. The secondary amine may be treated with a variety of agents suchas an aryl or alkyl isocyanate, acid chloride, sulfonyl chloride, orchloroformate to form the corresponding urea, amide, sulfonamide, orcarbamate intermediate A.

[0165] Intermediate A may be treated with OsO₄/NMMO/NaIO₄ to form thealdehyde intermediate B. Intermediate B is able to be converted to asecondary or tertiary amine via reductive amination using a primary orsecondary amine and Na(OAc)₃BH. The product can be cleaved from the acidlabile linker using TFA/CH₂Cl₂ to give the aryl compounds of theinvention.

[0166] When X=I or Br, intermediate A may be converted to a biarylcompound via Suzuki coupling (A. Suzuki et al, J. Amer. Chem. Soc., 111(1989) 314). using an arylboronic acid as shown in Scheme 4. The Suzukicoupling product can be treated with OsO₄/NMMO/NaIO₄ to convert theterminal olefin group to an aldehyde group. The resulting aldehyde isable to be converted to a secondary or tertiary amine via reductiveamination using a primary or secondary amine and Na(OAc)₃BH. The finalreaction product can be cleaved from the acid labile linker usingTFA/CH₂Cl₂ to give the biaryl compounds of the invention.

[0167] Scheme 5 outlines a general method for preparing compounds ofFormula I that feature functionalized R₁ groups derived from theintermediate B of Scheme 3. Thus, reductive amination of the aldehydeintermediate B using a Boc-protected diamine, for example,4N-tert-butyloxycarbonylaminopiperidine, forms a Boc-protected diaminecompound. Treatment of the resin with TMSOTf and 2,6-lutidine effectsclean removal of the Boc-protecting group with no cleavage of thecompound from the acid labile linker (ref.: A. J. Zhang et al, Tet.Lett. (1998), 39, 7439-7442. The resulting amine can then be derivatizedby reacting with an aryl or alkyl isocyanate, acid chloride sulfonylchloride, or chloroformate to form a corresponding urea, amide,sulfonamide, or carbamate intermediate C, respectively. Intermediate Cmay be cleaved directly from the acid labile linker using TFA/CH₂Cl₂ togive an aryl compound of Formula I of the invention. Alternatively,intermediate C may be converted to a biaryl compound via Suzuki couplingusing an arylboronic acid followed by treatment with TFA/CH₂Cl₂ to givea biaryl compound of Formula I of the invention.

[0168] Scheme 6 outlines a general method for preparing compounds ofFormula II of the invention using a novel solid phase synthesis. Thesynthesis commences with the coupling of a suitable linker, such asillustrated using an acid cleavable linker4-(4-formyl-3-methoxy-phenoxy)-butyric acid to a suitable amino resinthrough amide bond formation. Reductive amination of the linker aldehydewith a primary amine forms a resin bound secondary amine. The secondaryamine is then coupled with an acid chloride scaffold to form the amideintermediate D. Treatment of intermediate D with OSO₄/NMMO/NaIO₄converts the terminal olefin group to an aldehyde group. The aldehyde isable to be converted to a secondary or tertiary amine via reductiveamination using a primary or secondary amine and Na(OAc)₃BH. Cleavagefrom the acid labile linker using TFA/CH₂Cl₂ gives an aryl compound ofthe invention.

[0169] Alternatively, when X=I or Br, intermediate D may be treated withan aryl boronic acid via Suzuki coupling to form a biaryl compound asoutlined in Scheme 7. Reaction of the biaryl compound withOsO₄/NMMO/NaIO₄ converts the terminal olefin group to an aldehyde group.The resulting aldehyde is able to be converted to a secondary ortertiary amine via reductive amination using a primary or secondaryamine and Na(OAc)₃BH. Cleaved from the acid labile linker usingTFA/CH₂Cl₂ affords a biaryl compound of the invention.

[0170] Scheme 8 illustrates a general solution phase method forpreparing compounds of Formula II of the invention. Treatment of an acidchloride scaffold with an aniline gives the amide compound, which can beconverted to the biaryl intermediate via Suzuki coupling. Oxidation ofthe olefin followed by reductive amination provides biaryl compounds ofthe invention.

[0171] Scheme 9 outlines a method for preparing the cyclic urea(imidazolidinone) compounds of Formula I of the invention. The synthesisbegins with the heating of an aryl isocyanate in t-BuOH to form theBoc-protected aniline. Treatment of the aniline with NaH and allyliodide yields the Boc-protected N-allyl aniline. The olefin is thenconverted to an aldehyde via ozonolysis using O₃ followed by Me₂S. Theresulting aldehyde is combined with a 5-amino-4-aryl-4-alkyl-but-1-enesynthon through reductive amination to form a secondary amine. TheBoc-protecting group on the aniline nitrogen is removed using TFA/CH₂Cl₂and the resulting diamine is treated with CDI in toluene at reflux toform the cyclic urea intermediate. The olefin group in the cyclic ureaintermediate is converted to an aldehyde group via ozonolysis using O₃followed by Me₂S. Reductive amination of the resulting aldehyde with anappropriate primary or secondary amine provides the cyclic urea arylcompound of Formula I of the invention. When X is an iodo or bromogroup, reaction with arylboronic acids under Suzuki coupling conditionsgives the cyclic urea biaryl compound of the invention.

[0172] Scheme 10 outlines a method for preparing the series of carbamatecompounds of Formula II of the invention.

[0173] The synthesis starts with the oxidation of an appropriateiodophenylpentenenitrile to form an aldehyde using OsO₄/NMMO/NaIO₄.Reductive amination of the aldehyde with an appropriate secondary amine,such as dimethylamine, forms a tertiary amine. Suzuki coupling reactionis then performed to give the biaryl nitrile intermediate. Reduction ofthe nitrile intermediate using LiAIH₄ produced the alcohol product asshown in the scheme, presumably via an azetidinium cation intermediate.Treatment of the alcohol with an aryl isocyanate give the biarylcarbamate compound of Formula II of the invention.

[0174] The following Examples are provided for the purpose of furtherillustration only and are not intended to be limitations on thedisclosed invention. Examples 1-19 illustrate the synthesis of scaffoldintermediates.

EXAMPLE 1 (R,S) 2-(4-Bromophenyl)-pent-4-enylamine (General Procedure)

[0175]

[0176] 4-Bromophenylacetonitrile (10 g, 52.7 mmol, 1 eq) in THF (100 mL)was cooled to −78° C. under argon. LDA (2 M in THF, 29 mL, 58 mmol, 1.1eq) was added and the reaction was warmed to 0° C. over 1 h. Thereaction was re-cooled to −78° C. and allyl iodide (6.18 mL, 52.7 mmol,1 eq) was added and the reaction stirred at −78° C. for a further 2 h.The reaction was diluted with EtOAc (150 mL) and washed with aqueous HCI(1 M, 100 mL), aqueous Na₂S₂O₃ (100 mL) and saturated aqueous NaCI (100mL). The organic extracts were dried over anhydrous Na₂SO₄, filtered andconcentrated by rotary evaporation to afford crude1-cyano-1-(4-bromophenyl)-but-4-ene (10.5 g, ˜44 mmol) as a yellow oil.

[0177] A solution of LiAIH₄ (1 M in THF, 123 mL, 123 mmol) in THF (140mL) was cooled to 0° C. under Ar. H₂SO₄ (95%, 4 mL, 62.5 mmol) was addedin a drop-wise fashion over 10 min. The icebath was removed and themixture was stirred at room temperature for 2 h. A solution of crude1-cyano-1-(4bromophenyl)-but-4-ene (10.5 g, ˜44 mmol) in THF (60 mL) wasadded in a drop-wise fashion. The reaction was heated to reflux for 1 h,then cooled to room temperature and stirred for 16 h. The reaction wasquenched by careful addition of H₂O (4.67 mL, 260 mmol), NaOH (15%aqueous solution, 9.33 mL, 520 mmol ) and H₂O (14 mL, 780 mmol ). Theresulting slurry was diluted with EtOAc and stirred for a further 1 h,then filtered through a pad of celite 545®. The filtered salts werewashed with EtOAc (4×50 mL) and the filtrate was concentrated by rotaryevaporation to afford the title compound1-amino-2-(4-bromophenyl)-pent-5-ene as a dark brown oil (10.36 g, 43.1mmol, 88% over 2 steps): ¹H NMR (300 MHz, CDCl₃): δ 7.50 (dd, 2H), 7.30(d, 1H), 7.20 (d, 1H), 5.7 (m, 1H), 5.15 (m, 2H), 3.00 (m, 2H), 2.78 (m,1H), 2.50 (m, 2H), 1.70 (br s, 2H).

[0178] EXAMPLES 2-15 are listed in the following table: EXAMPLESTRUCTURE ¹H-NMR (300 MHz, CDCl₃) 2

7.75 (d, 2H), 7.05 (d, 2H), 5.75 (m, 1H), 5.11 (m, 2H), 3.08 (m, 1H),2.95 (m, 1H), 2.79 (m, 1H), 2.46 (m, 2H), 2.04 (br.s, 2H). 3

7.66 (m, 2H), 7.38 (m, 1H), 7.18 (m, 1H), 5.77 (m, 1H), 5.12 (m, 2H),3.02 (m, 2H), 2.75 (m, 1H), 2.49 (m, 2H), 1.56 (br.s, 2H). 4

7.30 (m, 4H), 5.78 (m, 1H), 5.10 (m, 2H), 3.09 (m, 1H), 2.95 (m, 1H),2.80 (m, 1H), 2.49 (m, 2H), 2.80 (m, 1H), 2.49 (m, 2H), 1.80 (br.s, 2H).5

7.23 (d, 2H), 7.11 (d, 2H), 5.61 (m, 1H), 4.98 (m, 2H), 2.90 (m, 2H),2.70 (m, 1H), 2.33 (m, 2H), 1.82 (br.s, 2H). 6

7.33 (m, 3H), 7.17 (m, 1H), 5.77 (m, 1H), 5.11 (m, 2H), 3.08 (m, 1H),2.96 (m, 1H), 2.79 (m, 1H), 2.49 (m, 2H), 1.43 (br.s, 2H). 7

7.51 (dd, 1H), 7.39 (dd, 1H), 7.15 (dd, 1H), 5.75 (m, 1H), 5.11 (m, 2H),3.08 (m, 1H), 2.95 (m, 1H), 2.78 (m, 1H), 2.48 (m, 2H), 1.68 (br.s, 2H).8

7.38 (m, 1H), 7.05 (m, 3H), 5.77 (m, 1H), 5.11 (m, 2H), 3.02 (m, 2H),2.81 (m, 1H), 2.48 (m, 2H), 1.50 (br.s, 2H). 9

7.14 (m, 3H), 5.72 (m, 1H), 5.08 (m, 2H), 3.06 (dd, 1H), 2.92 (dd, 1H),2.78 (m, 1H), 2.46 (m, 2H), 1.70 (br.s, 2H). 10

7.22 (dd, 4H), 5.80 (m, 1H), 5.11 (m, 2H), 3.07 (m, 1H), 2.95 (m, 1H),2.79 (m, 1H), 2.50 (m, 2H), 2.45 (s, 3H), 1.58 (br.s, 2H). 11

7.32 (m, 1H), 7.12 (m, 3H), 5.81 (m, 1H), 5.12 (m, 2H), 3.06 (m, 1H),2.96 (m, 1H), 2.77 (m, 1H), 2.48 (m, 2H), 2.47 (s, 3H), 1.62 (br.s, 2H).12

7.21 (m, 1H), 7.06 (m, 2H), 5.81 (m, 1H), 5.10 (m, 2H), 3.07 (m, 1H),2.94 (m, 1H), 2.76 (m, 1H), 2.48 (m, 2H), 2.36 (s, 3H), 2.34 (s, 3H),1.73 (br.s, 2H). 13

7.22 (d, 2H), 6.98 (d, 2H), 5.8 (m, 1H), 5.10 (m, 2H), 3.89 (s, 3H),2.98 (m, 2H), 2.76 (m, 1H), 2.48 (m, 2H), 1.43 (br.s, 2H). 14

6.80 (m, 3H), 6.20 (s, 2H), 5.79 (m, 1H), 5.08 (m, 2H), 3.02 (m, 1H),2.88 (m, 1H), 2.74 (m, 1H), 2.41 (m, 2H), 1.88 (br.s, 2H). 15

7.29 (m, 1H), 7.08 (m, 1H), 6.96 (m, 1H), 5.84 (m, 1H), 5.16 (m, 2H),3.16 (m, 1H), 3.12 (m, 2H), 2.57 (m, 2H), 1.66 (br.s, 2H).

EXAMPLE 16 2-(3,4-Dichlorophenyl)-2-mentyl-pent-4-enylamine

[0179]

[0180] 3,4-Dichlorophenylacetonitrile (5 g, 26.87 mmol, 1 eq) in THF (50mL) was cooled to −78° C. under Ar. LDA (2 M in THF, 16.1 mL, 32.2 mmol,1.2 eq) was added and the reaction was warmed to 0° C. over 1 h. Thereaction was re-cooled to −78° C. and allyl iodide (2.67 mL, 26.87 mmol,1 eq) was added then the reaction was stirred at −78° C. for a further 2h. The reaction was diluted with EtOAc (150 mL) and washed with aqueousHCI (1 M, 100 mL), saturated aqueous Na₂S₂O₃ (100 mL) and saturatedaqueous NaCI (100 mL). The organic extracts were dried over Na₂SO₄,filtered and concentrated by rotary evaporation to afford2-(3,4-dichlorophenyl)-pent-4-ene-nitrile (6.3 g, ˜28 mmol) as a yellowoil.

[0181] A 1 g (4.4 mmol) portion of2-(3,4-dichlorophenyl)-pent-4-ene-nitrile in THF is (25 mL) at −78° C.under Ar was treated with LDA (2M in THF, 2.7 mL, 5.4 mmol, 1.2 eq). Thereaction was warmed to 0° C. for 1 h, then recooled to −78° C. andmethyl iodide (0.28 mL, 4.4 mmol, 1.0 eq) was added. The reaction wasstirred at −78 ° C. for 1 h, then diluted with EtOAc and washed withaqueous HCI (1 M, 25 mL), aqueous Na₂S₂O₃ (25 mL) and saturated aqueousNaCI (25 mL). The organic extracts were dried over sodium sulfate,filtered and concentrated by rotary evaporation to afford2-(3,4-dichlorophenyl)-2-mentyl-pent-4-ene-nitrile (1.04 g, 4.39 mmol,99.8%) as a yellow oil. ¹H NMR (300 MHz, CDCl₃):δ 7.60 (dd,1H), 7.35 (m,2H), 5.77 (m, 1H), 5.28 (m, 2H), 2.72 (m, 2H), 1.8 (s, 3H).

[0182] A solution of LiAIH₄ (1 M in THF, 18.65 mL, 18.65 mmol,) in THF(25 mL) was cooled to 0° C. under Ar. H₂SO₄ (95 %, 0.51 mL, 9.38 mmol)was added in a dropwise fashion over 10 min. The mixture was stirred atroom temperature for 2 h, then a solution of2-(3,4-dichlorophenyl)-2-mentyl-pent-4-ene-nitrile (1.28 g, 6.22 mmol)in THF (10 mL) was added in a dropwise fashion. The reaction was heatedto reflux for 1 h, then cooled to room temperature and stirred for 16 h.The reaction was quenched by careful addition of H₂O (0.71 mL, 12.8mmol), NaOH (15% aqueous solution, 1.34 mL, 25.6 mmol) and H₂O (2.05 mL,38.4 mmol). The resulting slurry was stirred for a further 1 h and thenfiltered through a pad of celite 545®. The filtered salts were washedwith EtOAc (4×20 mL) and the combined organic filtrate was concentratedby rotary evaporation to afford the title compound1-amino-2-(3,4-dichlorophenyl)-2mentyl-pent-4enylamine (1.22g, 4.99mmol, 80.2%) as a dark brown oil. ¹H NMR (300 MHz, CDCl₃): δ 7.50(m,1H), 7.25 (m, 2H), 5.63 (m, 1H), 5.10 (m, 2H), 2.94 (dd, 2H), 2.54(m, 2H), 2.03 (brs, NH₂), 1.4 (s, 3H).

EXAMPLE 17 (R,S)-2-(3,4-Dichloro-phenyl)-pent-4-enoyl Chloride

[0183]

[0184] A solution of (3,4-dichlorophenyl)acetic acid (16.12 g, 78.5mmol) in MeOH (500 mL) was bubbled with HCI gas for 5 min. The mixturewas stirred at room temperature for 1 h. The solvent was removed byrotary evaporation and the. resulting residue was dissolved in EtOAc(400 mL) and washed with saturated aqueous NaHCO₃ (200 mL) and saturatedaqueous NaCI (200 mL). The organic extracts were dried over sodiumsulfate, filtered and concentrated by rotary evaporation to give(3,4-dichlorophenyl)acetic acid methyl ester (16.22 g, 74.1 mmol, 95%).¹H NMR (300 MHz, CDCl₃): δ 7.50 (m, 2H), 7.23 (dd,1H), 3.81 (s, 3H),3.69 (s, 2H).

[0185] (3,4-Dichloro-phenyl)-acetic acid methyl ester (5 g, 22.8 mmol)in THF (50 mL) was cooled to −78° C. under Ar. LDA (2M in THF, 13.7 mL,27.4 mmol, 1.2 eq) was added in a dropwise fashion and then the reactionwas warmed to 0° C. for 1 h. The reaction was cooled to −78° C. andallyl iodide (2.1 mL, 22.8 mmol, 1 eq) was added. The reaction wasstirred at −78° C. for 4 h and then diluted with EtOAc (200 mL), washedwith saturated aqueous Na₂S₂O₃ (100 mL) and saturated aqueous NaCl (100mL). The combined organic extracts were dried over Na₂SO₄, filtered andconcentrated by rotary evaporation to give crude(R,S)-2-(3,4-dichloro-phenyl)-pent-4-enoic acid methyl ester (6.0 g, ˜22mmol, 100%) as a brown oil. ¹H NMR (300 MHz, CDCl₃): δ 7.51 (m, 2H),7.26 (dd, 1H), 5.78 (m, 1H), 5.15 (m, 2H), 3.79 (s, 1H), 3.71 (m, 1H),2.90 (m,1H), 2.60 (m, 1H).

[0186] Lithium hydroxide (1.66 g, 69.3 mmol, 3 eq) was dissolved in H₂O(50 mL) and added to a solution of(R,S)-2-(3,4-dichloro-phenyl)-pent-4-enoic acid methyl ester (6 g, 22mmol) dissolved in THF/MeOH (1.5:1 v:v, 250 mL) and the resultingmixture was stirred at room temperature for 3 h. The solvent was removedby rotary evaporation and the residue was partitioned between EtOAc andH₂O. The aqueous layer was acidified to pH 3 with aqueous 6N HCI andextracted with EtOAc (2×100 mL). The combined organic extracts werewashed with saturated aqueous NaCI (100 mL) and concentrated by rotaryevaporation to give (R,S)-2-(3,4-dichloro-phenyl)-pent-4-enoic acid as abrown solid. ¹H NMR (300 MHz, CDCI₃): δ 7.52(m, 2H), 7.28(dd, 1H),5.79(m, 1H), 5.17(m, 2H), 3.73(t, 1H), 2.91(m, 1H), 2.62(m, 1H).

[0187] (R,S)-2-(3,4-Dichloro-phenyl)-pent-4-enoic acid (2.5 g, 10.24mmol, 1 eq) was dissolved in SOCl₂ (10 mL). The reaction mixture washeated to reflux for 1 h and then the SOCl₂ was removed by rotaryevaporation. The residue was co-evaporated from toluene (3×5 mL) andthen dried under high vacuum for 1 h. It was redissolved in toluene (1mL) and concentrated by rotary evaporation and then dried under highvacuum for 4 h to give the title compound(R,S)-2-(3,4-dichloro-phenyl)-pent-4-enoyl chloride (2.69 g, 10.2 mmol,˜100%). The acid chloride was used directly in the solid phase synthesisreactions.

[0188] EXAMPLES 18-19 are listed in the following table: EXAMPLESTRUCTURE ¹H-NMR (300 MHz, CDCl₃) 18

7.58 (d, 2H), 7.32 (d, 2H), 5.81 (m, 1H), 5.16 (m, 2H), 3.73 (dd, 1H),2.90 (m, 1H), 2.63 (m, 1H). 19

7.52 (m, 2H), 7.28 (dd, 1H), 5.79 (m, 1H), 5.17 (m, 2H), 3.73 (t, 1H),2.91 (m, 1H), 2.62 (m, 1H).

[0189] Examples 20-33 illustrate the synthesis of MCH active compounds.

EXAMPLE 20(R,S)-N-[4-Cyclopentylamino-2-(3,4-dichloro-phenyl)-butyl]-3,5-bis-trifluoromethyl-benzamide

[0190]

[0191] A 1 liter bottle was charged with Argo-Gel-NH₂ (30 g, 12 mmol,supplied by Argonaut Technologies, Incorporated, California), CH₂CI₂(200 mL) and DMF (50 mL). A premixed (30 min) solution of4-(4-formyl-3-methoxy-phenoxy)-butyric acid linker (8.577 g, 36 mmol, 3eq), HOBt (4.865 g, 36 mmol, 3 eq) and DIC (11.54 mL, 72 mmol, 6 eq) inCH₂CI₂ (250 mL) was added to the resin suspension and the mixture wasshaken at room temperature for 16 h. The resin was transferred to 2large shaking vessels, the solution was drained and the resin was washedwith DMF (3×), MeOH (3×) and CH₂CI₂ (3×) and dried under high vacuum togive the acid cleavable linker containing4-(4-formyl-3-methoxy-phenoxy)-butyramide resin.

[0192] A 100 mg (0.04 mmol) portion of the resin was suspended inCICH₂CH₂CI (1 mL) and a solution of1-amino-2-(3,4-dichloro-phenyl)-pent-5-ene (0.05 g, 0.2 mmol, 5 eq) inCICH₂CH₂CI (1 mL) was added. The resin was shaken for 20 min at roomtemperature and then Na(OAc)₃BH (0.045 g, 0.2 mmol, 5 eq) was added andthe reaction was shaken at room temperature for 16 h. The solution wasfiltered and the resin was washed with MeOH (1×), DMF (3×), MeOH (3×)and CH₂CI₂ (3×). An aliquot of the resin tested positive with chloraniland negative with 2,4-dinitrophenylhydrazine.

[0193] The resin was suspended in pyridine (1.5 mL) and3,5bis(trifluoromethyl)-benzoyl chloride (1.5 mL of a 1 M solution inCH₂CI₂, 1.5 mmol) was added. The resin was shaken at room temperaturefor 16 h, the solution filtered and the resin washed with CH₂CI₂ (3×),DMF (3×), MeOH (2×) and CH₂CI₂ (3×). An aliquot of the resin gave anegative chloranil test.

[0194] The resin was shaken at room temperature for 14 h with a solutionof OsO₄ (4% in H₂O, 0.052 mL, 0.008 mmol, 0.2 eq) and NMMO (0.05 g, 0.4mmol, 10 eq) in acetone-H₂O (1:1, 3 mL) at room temperature for 14 h.The solution was filtered and the resin was washed with H₂O (2×),acetone (2×), pyridine (1×, shake for 30 min), MeOH (2×) and CH₂CI₂(3×). A solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) in acetone-H₂O(1:1, 3 mL) was added and the mixture shaken for 2 h. The solution wasfiltered and the resin was washed with H₂O (2×) and acetone (1×). Theresin was treated with a fresh solution of NaIO₄ (0.085 g, 0.4 mmol, 10eq) in acetone-H₂O (1:1, 3 mL) and shaken for a further 2 h. Thesolution was filtered and the resin was washed with H₂O (3×), acetone(1X), MeOH (2×) and CH₂CI₂ (3×).

[0195] The resin was shaken with a solution of cyclopentylamine (0.024g, 0.2 mmol, 5 eq) in CICH₂CH₂CI (1.5 mL) for 30 min. Na(OAc)₃BH (0.05g, 0.2 mmol, 5 eq) was added and the mixture shaken at room temperaturefor 14 h. The solution was filtered and the resin washed with MeOH (2×),DMF (3×), MeOH (3×) and CH₂CI₂ (3×). An aliquot of the resin gave apositive chloranil test. The resin was treated with a solution of TFA(25% in CH₂CI₂, 3 mL) and shaken for 2 h at room temperature, filteredoff and the filtrate was purified by Gilson 215 HPLC (10-90%acetonitrile/water) to yield the title compound (0.0050 g, 27%), MS(ESI): 541.1 (M+1), 543.1 (M+3).

EXAMPLE 21(R,S)-3,4-Dichloro-N-[4-cyclopentylamino-2-(3,4-dichloro-phenyl)-butyl]-benzenesulfonamide

[0196]

[0197] A 100 mg (0.04 mmol) portion of the4-(4-formyl-3-methoxy-phenoxy)-butyramide resin (see step 1 of EXAMPLE20) was suspended in CICH₂CH₂CI (1 mL) and a solution of1-amino-2-(3,4-dichloro-phenyl)-pent-5-ene (0.05 g, 0.2 mmol, 5 eq) inCICH₂CH₂CI (1 mL) was added. The resin was shaken for 20 min at roomtemperature and then Na(OAc)₃BH (0.045 g, 0.2 mmol, 5 eq) was added. Thereaction was shaken at room temperature for 16 h. The solution wasfiltered and the resin was washed with MeOH (1X), DMF (3×), MeOH (3×)and CH₂CI₂ (3×). An aliquot of the resin tested positive with chloraniland negative with 2,4-dinitrophenylhydrazine.

[0198] The resin was suspended in pyridine (1.5 mL) and3,4-dichlorobenzenesulfonyl chloride (1.5 mL of a 1 M solution inCH₂CI₂, 1.5 mmol) was added. The resin was shaken at room temperaturefor 16 h, the solution filtered and the resin washed with CH₂CI₂ (3×),DMF (3×), MeOH (2×) and CH₂CI₂ (3×). An aliquot of the resin gave anegative chloranil test.

[0199] The resin was shaken at room temperature for 14 h with a solutionof OSO₄ (4% in H₂O, 0.052 mL, 0.008 mmol, 0.2 eq) and NMMO (0.05 g, 0.4mmol, 10 eq) in acetone-H₂O (1:1, 3 mL) at room temperature for 14 h.The solution was filtered and the resin was washed with H₂O (2×),acetone (2×), pyridine (1×, shake for 30 min), MeOH (2×) and CH₂CI₂(3×). A solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) in acetone-H₂O(1:1, 3 mL) was added and the mixture shaken for 2 h. The solution wasfiltered and the resin was washed with H₂O (2×), acetone (1×). The resinwas treated with a fresh solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) inacetone-H₂O (1:1, 3 mL) and shaken for a further 2 h. The solution wasfiltered and the resin was washed with H₂O (3×), acetone (1×), MeOH (2×)and CH₂CI₂ (3×).

[0200] The resin was shaken with a solution of cyclopentylamine (0.024g, 0.2 mmol, 5 eq) in CICH₂CH₂CI (1.5 mL) for 30 min. Na(OAc)₃BH (0.05g,0.2 mmol, 5 eq) was added and the mixture shaken at room temperature for14 h. The solution was filtered and the resin washed with MeOH (2×), DMF(3×), MeOH (3×) and CH₂CI₂ (3×). An aliquot of the resin gave a positivechloranil test. The resin was treated with a solution of TFA (TFA, 25%in CH₂CI₂, 3 mL) and shaken for 2 h at room temperature, filtered offand the filtrate was purified by Gilson 215 HPLC (10-90%acetonitrile/water) to yield the title compound (0.00102 g, 47%). MS(ESI): 509.1 (M+1), 511.0 (M+3), 513.0 (M+5).

EXAMPLE 22(R,S)-[3-Cyclobutylamino-2-(3,4-dichloro-phenyl)-propyl]-3-(4-fluoro-3-nitro-phenyl)-urea

[0201]

[0202] A 100 mg (0.04 mmol) portion of the4-(4-formyl-3-methoxy-phenoxy)-butyramide resin (see step 1 of EXAMPLE20) was suspended in CICH₂CH₂CI (1 mL) and a solution of1-amino-2-(3,4-dichloro-phenyl)-pent-5-ene (0.047 g, 0.2 mmol, 5 eq) inCICH₂CH₂CI (1 mL) was added. The resin was shaken for 20 min at roomtemperature and then Na(OAc)₃BH (0.045 g, 0.2 mmol, 5 eq) was added. Thereaction was shaken at room temperature for 16 h. The solution wasfiltered and the resin was washed with MeOH (1×), DMF (3×), MeOH (3×)and CH₂CI₂ (3×). An aliquot of the resin tested positive with chloraniland negative with 2,4-dinitrophenylhydrazine.

[0203] The resin was suspended in CH₂CI₂ (3.0 mL) and DIEA (0.035 mL, 5eq) was added, followed by 3-nitro-4-fluorophenyl isocyanate (0.217 mL,1.5 mmol).

[0204] The mixture was shaken at room temperature for 16 h, the solutionfiltered and the resin washed with CH₂CI₂ (3×), DMF (3×), MeOH (2×) andCH₂CI₂ (3×). An aliquot of the resin gave a negative chloranil test.

[0205] The resin was shaken at room temperature for 14 h with a solutionof OSO₄ (4% in H₂O, 0.052 mL, 0.008 mmol, 0.2 eq) and NMMO (0.05 g, 0.4mmol, 10 eq) in acetone-H₂O (1:1, 3 mL) at room temperature for 14 h.The solution was filtered and the resin was washed with H₂O (2×),acetone (2×), pyridine (1×, shake for 30 min), MeOH (2×) and CH₂CI₂(3×). A solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) in acetone-H₂O(1:1, 3 mL) was added and the mixture shaken for 2 h. The solution wasfiltered and the resin was washed with H₂O (2×), acetone (1×). The resinwas treated with a fresh solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) inacetone-H₂O (1:1, 3 mL) and shaken for a further 2 h. The solution wasfiltered and the resin was washed with H₂O (3×), acetone (1×), MeOH (2×)and CH₂CI₂ (3×).

[0206] The resin was shaken with a solution of cyclobutylaminehydrochloride (0.022 g, 0.2 mmol, 5 eq) and triethylamine (0.03 mL, 0.2mmol) in CICH₂CH₂CI (1.5 mL) for 30 min. Na(OAc)₃BH (0.05 g, 0.2 mmol, 5eq) was added and the mixture shaken at room temperature for 14 h. Thesolution was filtered and the resin washed with MeOH (2×), DMF (3×),MeOH (3×) and CH₂CI₂ (3×). An aliquot of the resin gave a positivechloranil test. The resin was treated with a solution of TFA (25% inCH₂CI₂, 3 mL) and shaken for 2 h at room temperature, filtered off andthe filtrate was purified by Gilson 215 HPLC (10-90% acetonitrile/water)to yield the title compound (0.0062 g, 33%). MS (ESI): 469.0 (M+1),471.0 (M+3).

EXAMPLE 23(R,S)-1-[2-(3-Cyano-biphenyl-4-yl)-4-cyclopentylamino-butyl]-3-(3,5-dichloro-phenyl)-urea

[0207]

[0208] A 100 mg (0.04 mmol) portion of the4-(4-formyl-3-methoxy-phenoxy) butyramide resin (see step 1 of EXAMPLE20) was suspended in CICH₂CH₂CI (1 mL) and a solution of1-amino-2-(4-bromophenyl)-pent-5-ene (0.048 g, 0.2 mmol, 5 eq) inCICH₂CH₂CI (1 mL) was added. The resin was shaken for 20 min at roomtemperature and then Na(OAc)₃BH (0.045 g, 0.2 mmol, 5 eq) was added. Thereaction was shaken at room temperature for 16 h. The solution wasfiltered and the resin was washed with MeOH (1×), DMF (3×), MeOH (3×)and CH₂CI₂ (3×). An aliquot of the resin tested positive with chloraniland negative with 2,4-dinitrophenylhydrazine.

[0209] The resin was suspended in CH₂CI₂ (3.0 mL) and DIEA (0.035 mL,0.2 mmol, 5 eq) was added, followed by 3,5-dichloro-phenyl isocyanate(0.283 g, 1.5 mmol, to give a 0.5M solution). The mixture was shaken atroom temperature for 16 h, the solution filtered and the resin washedwith CH₂CI₂ (3×), DMF (3×), MeOH (2×) and CH₂CI₂ (3×). An aliquot of theresin gave a negative chloranil test.

[0210] The resin was mixed with 3-cyanophenylboronic acid (0.024 g, 0.16mmol, 4 eq), K₂CO₃ (0.028 g, 0.2 mmol, 5 eq) and Pd(PPh₃)₄ (0.009 g,0.008 mmol, 0.2 eq). DMF (2 mL, degassed with Ar) was added and themixture was heated to 70° C. for 16 h. The solution was filtered and theresin washed with DMF (4×), H₂O (4×), MeOH (3×) and CH₂CI₂ (4×).

[0211] The resin was shaken at room temperature for 14 h with a solutionof OSO₄ (4% in H₂O, 0.052 mL, 0.008 mmol, 0.2 eq) and NMMO (0.05 g, 0.4mmol, 10 eq) in acetone-H₂O (1:1, 3 mL) at room temperature for 14 h.The solution was filtered and the resin was washed with H₂O (2×),acetone (2×), pyridine (1×, shake for 30 min), MeOH (2×) and CH₂CI₂(3×). A solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) in acetone-H₂O(1:1, 3 mL) was added and the mixture shaken for 2 h. The solution wasfiltered and the resin was washed with H₂O (2×), acetone (1×). The resinwas treated with a fresh solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) inacetone-H₂O (1:1, 3 mL) and shaken for a further 2 h. The solution wasfiltered and the resin was washed with H₂O (3×), acetone (1×), MeOH (2×)and CH₂CI₂ (3×).

[0212] The resin was shaken with a solution of cyclopentylamine (0.02mL, 0.2 mmol, 5 eq) in CICH₂CH₂CI (1.5 mL) for 30 min. Na(Oac)₃BH (0.05g, 0.2 mmol, 5 eq) was added and the mixture shaken at room temperaturefor 14 h. The solution was filtered and the resin washed with MeOH (2×),DMF (3×), MeOH (3×) and CH₂CI₂ (3×). An aliquot of the resin gave apositive chloranil test. The resin was treated with a solution of TFA(25% in CH₂CI₂, 3 mL) and shaken for 2 h at room temperature, filteredoff and the filtrate was purified by Gilson 215 HPLC (10-90%acetonitrile/water) to yield (R,S )-1-[2-(3′-Cyano-biphenyl-4-yl)-4cyclopentylamino-butyl]-3-(3,5-dichloro-phenyl)urea (0.092 g, 44%).¹H NMR (300 MHz, CDCI₃): δ 7.72 (m, 2H), 7.51 (m,1H), 7.44 (m, 3H), 7.24(m, 4H), 6.80 (dd,1H), 3.26 (m, 3H), 2.84 (m,1H), 2.65 (m, 2H), 2.05(m,1H), 1.88 (m, 3H), 1.65 (m, 2H), 1.47 (m, 3H); MS (ESI): 521.0 (M+1),523.0 (M+3).

EXAMPLE 24(R,S)-N-[2-(3′-Cyano-biphenyl-4-yl)-4-methylamino-butyl]-3,4-difluoro-benzamide

[0213]

[0214] A 100 mg (0.04 mmol) portion of the4-(4-formyl-3-methoxy-phenoxy) butyramide resin (see step 1 of EXAMPLE20) was suspended in CICH₂CH₂CI (1 mL) and a solution of1-amino-2-(4iodophenyl)-pent-5-ene (0.05 g, 0.2 mmol, 5 eq) inCICH₂CH₂CI (1 mL) was added. The resin was shaken for 20 min at roomtemperature and then Na(Oac)₃BH (0.045 g, 0.2 mmol, 5 eq) was added. Thereaction was shaken at room temperature for 16 h. The solution wasfiltered and the resin was washed with MeOH (1×), DMF (3×), MeOH (3×)and CH₂CI₂ (3×). An aliquot of the resin tested positive with chloraniland negative with 2,4-dinitrophenylhydrazine.

[0215] The resin was suspended in pyridine (1.5 mL) and3,4difluorobenzoyl chloride (1.5 mL of a 1 M solution in CH₂CI₂, 1.5mmol) was added. The resin was shaken at room temperature for 16 h, thesolution filtered and the resin washed with CH₂CI₂ (3×), DMF (3×), MeOH(2×) and CH₂CI₂ (3×). An aliquot of the resin gave a negative chloraniltest.

[0216] To the resin was added 3-cyanophenylboronic acid (0.024 g, 0.16mmol, 4 eq), K₂CO₃ (0.028 g, 0.2 mmol, 5 eq) and Pd(PPh₃)₄ (0.009 g,0.008 mmol, 0.2 eq). DMF (2 mL, degassed with Ar) was added and themixture was heated to 70° C. for 16 h. The solution was filtered and theresin washed with DMF (4×), H₂O (4×), MeOH (3×) and CH₂CI₂ (4×).

[0217] The resin was shaken at room temperature for 14 h with a solutionof OsO₄ (4% in H₂O, 0.052 mL, 0.008 mmol, 0.2 eq) and NMMO (0.05 g, 0.4mmol, 10 eq) in acetone-H₂O (1:1, 3 mL) at room temperature for 14 h.The solution was filtered and the resin was washed with H₂O (2×),acetone (2×), pyridine (1×, shake for 30 min), MeOH (2×) and CH₂CI₂(3×). A solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) in acetone-H₂O(1:1, 3 mL) was added and the mixture shaken for 2 h. The solution wasfiltered and the resin was washed with H₂O (2×), acetone (1×). The resinwas treated with a fresh solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) inacetone-H₂O (1:1, 3 mL) and shaken for a further 2 h. The solution wasfiltered and the resin was washed with H₂O (3×), acetone (1×), MeOH (2×)and CH₂CI₂ (3×).

[0218] The resin was shaken with a solution of methylamine (0.21 mL, 2Msolution, 0.4 mmol, 10 eq) in CICH₂CH₂CI (1.5 mL) for 30 min. Na(OAc)₃BH(0.05 g, 0.2 mmol, 5 eq) was added and the mixture shaken at roomtemperature for 14 h. The solution was filtered and the resin washedwith MeOH (2×), DMF (3×), MeOH (3×) and CH₂CI₂ (3×). An aliquot of theresin gave a positive chloranil test. The resin was treated with asolution of TFA (25% in CH₂CI₂, 3 mL) and shaken for 2 h at roomtemperature, filtered off and the filtrate was purified by Gilson 215HPLC (10-90% acetonitrile/water) to yield the title compound (0.0019 g,11%). MS (ESI): 420.1 (M+1),421.1 (M+2).

EXAMPLE 25(R,S)-3,5-Dichloro-N[2-(3′-cyano-biphenyl-4-yl)-4dimethylaminobutyl]benzenesulfonamide

[0219]

[0220] A 100 mg (0.04 mmol) portion of the4-(4-formyl-3-methoxy-phenoxy) butyramide resin (see step 1 of EXAMPLE20) was suspended in CICH₂CH₂CI (1 mL) and a solution of1-amino-2-(4iodophenyl)-pent-5-ene (0.05 g, 0.2 mmol, 5 eq) inCICH₂CH₂CI (1 mL) was added. The resin was shaken for 20 min at roomtemperature and then Na(OAc)₃BH (0.045 g, 0.2 mmol, 5 eq) was added. Thereaction was shaken at room temperature for 16 h. The solution wasfiltered and the resin was washed with MeOH (1×), DMF (3×), MeOH (3×)and CH₂CI₂ (3×). An aliquot of the resin tested positive with chloraniland negative with 2,4-dinitrophenylhydrazine.

[0221] The resin was suspended in pyridine (1.5 mL) and3,5-dichlorobenzenesulfonyl chloride (1.5 mL of a 1 M solution inCH₂CI₂, 1.5 mmol) was added. The resin was shaken at room temperaturefor 16 h, the solution filtered and the resin washed with CH₂CI₂ (3×),DMF (3×), MeOH (2×) and CH₂CI₂ (3×). An aliquot of the resin gave anegative chloranil test.

[0222] The resin was shaken at room temperature for 14 h with a solutionof OsO₄ (4% in H₂O, 0.052 mL, 0.008 mmol, 0.2 eq) and NMMO (0.05 g, 0.4mmol, 10 eq) in acetone-H₂O (1:1, 3 mL) at room temperature for 14 h.The solution was filtered and the resin was washed with H₂O (2×),acetone (2×), pyridine (1×, shake for 30 min), MeOH (2×) and CH₂CI₂(3×). A solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) in acetone-H₂O(1:1, 3 mL) was added and the mixture shaken for 2 h. The solution wasfiltered and the resin was washed with H₂O (2×), acetone (1×). The resinwas treated with a fresh solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) inacetone-H₂O (1:1, 3 mL) and shaken for a further 2 h. The solution wasfiltered and the resin was washed with H₂O (3×), acetone (1×), MeOH (2×)and CH₂CI₂ (3×).

[0223] The resin was shaken with a solution of dimethylamine (0.10 mL ofa 2 M solution in THF, 0.2 mmol, 5 eq) in CICH₂CH₂CI (1.5 mL) for 30min. Na(OAc)₃BH (0.05 g, 0.2 mmol, 5 eq) was added and the mixtureshaken at room temperature for 14 h. The solution was filtered and theresin washed with MeOH (2×), DMF (3×), MeOH (3×) and CH₂CI₂ (3×). Analiquot of the resin gave a positive chloranil test.

[0224] The resin was treated with a solution of TFA (TFA, 25% in CH₂CI₂,3 mL) and shaken for 2 h at room temperature, filtered off and thefiltrate was purified by Gilson 215 HPLC (1090% acetonitrile/water) toyield the title compound (0.0024 g, 12%). MS (ESI): 502.1/504.1 (M+1).

EXAMPLE 26(R,S)-[-2-(3′-Cyano-biphenyl-4-yl)-4-isopropylaminobutyl]-carbamicacid-4-chlorophenyl ester

[0225]

[0226] A 100 mg (0.04 mmol) portion of the4-(4-formyl-3-methoxy-phenoxy) butyramide resin (see step 1 of EXAMPLE20) was suspended in CICH₂CH₂CI (1 mL) and a solution of1-amino-2-(4iodophenyl)-pent-5-ene (0.05 g, 0.2 mmol, 5 eq) inCICH₂CH₂CI (1 mL) was added. The resin was shaken for 20 min at roomtemperature and then Na(OAc)₃BH (0.045 g, 0.2 mmol, 5 eq) was added. Thereaction was shaken at room temperature for 16 h. The solution wasfiltered and the resin was washed with MeOH (1×), DMF (3×), MeOH (3×)and CH₂CI₂ (3×). An aliquot of the resin tested positive with chloraniland negative with 2,4-dinitrophenylhydrazine.

[0227] The resin was suspended in pyridine (1.5 mL) and 4chlorophenylchloroformate (1.5 mL of a 1 M solution in CH₂CI₂, 1.5 mmol) was added.The resin was shaken at room temperature for 16 h, the solution filteredand the resin washed with CH₂CI₂ (3×), DMF (3×), MeOH (2×) and CH₂CI₂(3×). An aliquot of the resin gave a negative chloranil test.

[0228] The resin was shaken at room temperature for 14 h with a solutionof OsO₄ (4% in H₂O, 0.052 mL, 0.008 mmol, 0.2 eq) and NMMO (0.05 g, 0.4mmol, 10 eq) in acetone-H₂O (1:1, 3 mL) at room temperature for 14 h.The solution was filtered and the resin was washed with H₂O (2×),acetone (2×), pyridine (1×, shake for 30 min), MeOH (2×) and CH₂CI₂(3×). A solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) in acetone-H₂O(1:1, 3 mL) was added and the mixture shaken for 2 h. The solution wasfiltered and the resin was washed with H₂O (2×), acetone (1×). The resinwas treated with a fresh solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) inacetone-H₂O (1:1, 3 mL) and shaken for a further 2 h. The solution wasfiltered and the resin was washed with H₂O (3×), acetone (1×), MeOH (2×)and CH₂CI₂ (3×).

[0229] The resin was shaken with a solution of isopropylamine (0.02 mL ,0.2 mmol, 5 eq) in CICH₂CH₂CI (1.5 mL) for 30 min. Na(OAc)₃BH (0.05g,0.2 mmol, 5 eq) was added and the mixture shaken at room temperature for14 h. The solution was filtered and the resin washed with MeOH (2×), DMF(3×), MeOH (3×) and CH₂CI₂ (3×). An aliquot of the resin gave a positivechloranil test. The resin was treated with a solution of TFA (TFA, 25%in CH₂CI₂, 3 mL) and shaken for 2 h at room temperature, filtered offand the filtrate was purified by Gilson 215 HPLC (1090%acetonitrile/water) to yield the title compound (0.0027 g, 15%). MS(ESI): 460.1/462.2 (M+1).

EXAMPLE 27(R,S)-1-1-{3-(3′-Cyano-biphenyl-4-yl)-4-[3(3,5-dichloro-phenyl)ureido]-butyl}pyrrolidin-3-yl)-3ethyl-urea

[0230]

[0231] A 100 mg (0.04 mmol) portion of the4-(4-formyl-3-methoxy-phenoxy)-butyramide resin (see step 1 of EXAMPLE20) was suspended in CICH₂CH₂CI (1 mL) and a solution of1-amino-2-(4-bromophenyl)-pent-5-ene (0.048 g, 0.2 mmol, 5 eq) inCICH₂CH₂CI (1 mL) was added. The resin was shaken for 20 min at roomtemperature and then Na(OAc)₃BH (0.045 g, 0.2 mmol, 5 eq) was added. Thereaction was shaken at room temperature for 16 h. The solution wasfiltered and the resin was washed with MeOH (1×), DMF (3×), MeOH (3×)and CH₂CI₂ (3×). An aliquot of the resin tested positive with chloraniland negative with 2,4-dinitrophenylhydrazine.

[0232] The resin was suspended in CH₂CI₂ (3.0 mL) and DIEA (0.035 mL,0.2 mmol, 5 eq) was added followed by 3,5-dichloro-phenyl isocyanate(10.283 g, 1.5 mmol, to give a 0.5 M solution). The resin was shaken atroom temperature for 16 h, the solution filtered and the resin washedwith CH₂CI₂ (3×), DMF (3×), MeOH (2×) and CH₂CI₂ (3×). An aliquot of theresin gave a negative chloranil test.

[0233] To the resin was added 3-cyanophenylboronic acid (0.024 g, 0.16mmol, 4 eq), K₂CO₃ (0.028 g, 0.2 mmol, 5 eq) and Pd(PPh₃)₄ (0.009 g,0.008 mmol, 0.2 eq). DMF (2 mL, degassed with Ar) was added and themixture was heated to 70° C. for 16 h. The solution was filtered and theresin washed with DMF (4×), H₂O (4×), MeOH (3×) and CH₂CI₂ (4×).

[0234] The resin was shaken at room temperature for 14 h with a solutionof OsO₄ (4% in H₂O, 0.052 mL, 0.008 mmol, 0.2 eq) and NMMO (0.05 g, 0.4mmol, 10 eq) in acetone-H₂O (1:1, 3 mL) at room temperature for 14 h.The solution was filtered and the resin was washed with H₂O (2×),acetone (2×), pyridine (1×, shake for 30 min), MeOH (2×) and CH₂CI₂(3×). A solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) in acetone-H₂O(1:1, 3 mL) was added and the mixture shaken for 2 h. The solution wasfiltered and the resin was washed with H₂O (2×), acetone (1×). The resinwas treated with a fresh solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) inacetone-H₂O (1:1, 3 mL) and shaken for a further 2 h. The solution wasfiltered and the resin was washed with H₂O (3×), acetone (1×), MeOH (2×)and CH₂CI₂ (3×).

[0235] The resin was shaken with a solution of pyrrolidin3-yl-carbamicacid tert butyl ester (0.037 g, 0.2 mmol, 5 eq) in CICH₂CH₂CI (1.5 mL)for 30 min. Na(OAc)₃BH (0.05 g, 0.2 mmol, 5 eq) was added and themixture shaken at room temperature for 14 h. The solution was filteredand the resin washed with MeOH (2×), DMF (3×), MeOH (3×) and CH₂CI₂(3×).

[0236] The resin was suspended in CH₂CI₂ (3 mL) and treated with2,6lutidine (0.52 mL, 4.5 mmol, 1.5M final concentration) and TMSOTf(0.54 mL, 3 mmol, 1 M final concentration). The mixture was shaken atroom temperature for 1 h. The mixture was drained and the resin washedwith CH₂CI₂ (3×), MeOH (3×) and CH₂CI₂ (3×). An aliquot of the resingave a positive ninhydrin test.

[0237] The resin was suspended in CH₂CI₂ (3 mL) and treated with ethylisocyanate (0.19 mL, 1.5 mmol, 0.5M final concentration) and DIEA (0.035mL, 0.2 mmol, 5 eq). The mixture was shaken at room temperature for 14 hand then the solution was filtered and the resin was washed with DMF(3×), MeOH (3×) and CH₂CI₂ (3×).

[0238] The resin was treated with a solution of TFA (25% in CH₂CI₂, 3mL) and shaken for 2 h at room temperature, filtered off and thefiltrate was purified by Gilson 215 HPLC (1090% acetonitrile/water) toyield the title compound (0.0011 g, 5%). MS(ESI): 593.1 (M+1), 595.1(M+3).

EXAMPLE 28(R,S)-3,5-Dichloro-N(1-{3-(3′-cyano-biphenyl-4-yl)-4-[3-(3,5-dichloro-phenyl)ureido]butyl}pyrrolidin-3-yl)-benzamide

[0239]

[0240] A 100 mg (0.04 mmol) portion of the4-(4-formyl-3-methoxy-phenoxy) butyramide resin (see step 1 of EXAMPLE20) was suspended in CICH₂CH₂CI (1 mL) and a solution of1-amino-2-(4-bromophenyl)-pent-5-ene (0.048 g, 0.2 mmol, 5 eq) inCICH₂CH₂CI (1 mL) was added. The resin was shaken for 20 min at roomtemperature and then Na(OAc)₃BH (0.045 g, 0.2 mmol, 5 eq) was added. Thereaction was shaken at room temperature for 16 h. The solution wasfiltered and the resin was washed with MeOH (1×), DMF (3×), MeOH (3×)and CH₂CI₂ (3×). An aliquot of the resin tested positive with chloraniland negative with 2,4-dinitrophenylhydrazine.

[0241] The resin was suspended in CH₂CI₂ (3.0 mL) and DIEA (0.035 mL,0.2 mmol, 5 eq) was added followed by 3,5-dichloro-phenyl isocyanate(10.283 g, 1.5 mmol, to give a 0.5 M solution). The resin was shaken atroom temperature for 16 h, the solution filtered and the resin washedwith CH₂CI₂ (3×), DMF (3×), MeOH (2×) and CH₂CI₂ (3×). An aliquot of theresin gave a negative chloranil test.

[0242] To the resin was added 3-cyanophenylboronic acid (0.024 g, 0.16mmol, 4 eq), K₂CO₃ (0.028 g, 0.2 mmol, 5 eq) and Pd(PPh₃)₄ (0.009 g,0.008 mmol, 0.2 eq). DMF (2 mL, degassed with Ar) was added and themixture was heated to 70° C. for 16 h. The solution was filtered and theresin washed with DMF (4×), H₂O (4×), MeOH (3×) and CH₂CI₂ (4×).

[0243] The resin was shaken at room temperature for 14 h with a solutionof OsO₄ (4% in H₂O, 0.052 mL, 0.008 mmol, 0.2 eq) and NMMO (0.05 g, 0.4mmol, 10 eq) in acetone-H₂O (1:1, 3 mL) at room temperature for 14 h.The solution was filtered and the resin was washed with H₂O (2×),acetone (2×), pyridine (1×, shake for 30 min), MeOH (2×) and CH₂CI₂(3×). A solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) in acetone-H₂O(1:1, 3 mL) was added and the mixture shaken for 2 h. The solution wasfiltered and the resin was washed with H₂O (2×), acetone (1×). The resinwas treated with a fresh solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) inacetone-H₂O (1:1, 3 mL) and shaken for a further 2 h. The solution wasfiltered and the resin was washed with H₂O (3×), acetone (1×), MeOH (2×)and CH₂CI₂ (3×).

[0244] The resin was shaken with a solution of pyrrolidin3-yl-carbamicacid tert butyl ester (0.037 g, 0.2 mmol, 5 eq) in CICH₂CH₂CI (1.5 mL)for 30 min. Na(OAc)₃BH (0.05 g, 0.2 mmol, 5 eq) was added and themixture shaken at room temperature for 14 h. The solution was filteredand the resin washed with MeOH (2×), DMF (3×), MeOH (3×) and CH₂CI₂(3×).

[0245] The resin was suspended in CH₂CI₂ (3 mL) and treated with2,6lutidine (0.52 mL, 4.5 mmol, 1.5M final concentration) and TMSOTf(0.54 mL, 3 mmol, 1 M final concentration). The mixture was shaken atroom temperature for 1 h. The mixture was drained and the resin washedwith CH₂CI₂ (3×), MeOH (3×) and CH₂CI₂ (3×). An aliquot of the resingave a positive ninhydrin test.

[0246] The resin was suspended in CH₂CI₂ (1.5 mL) and treated with3,5-dichloro-benzoyl chloride (0.315 g, 1.5 mmol) and pyridine (1.5 mL).The mixture was shaken at room temperature for 14 h and then thesolution was filtered and the resin was washed with DMF (3×), MeOH (3×)and CH₂CI₂ (3×).

[0247] The resin was treated with a solution of TFA (25% in CH₂CI₂, 3mL) and shaken for 2 h at room temperature, filtered off and thefiltrate was purified by Gilson 215 HPLC (10-90% acetonitrile/water) toyield the title compound (0.0023 g, 9%). MS(ESI): 693.9/695.9/697.9(M+1).

EXAMPLE 29(R,S)-N-(1-{3-(3′-Cyano-biphenyl-4-yl)-4-[3-(3,5-dichloro-phenyl)ureido]-

[0248]

butyl}-piperidin-4-yl)methane-sulfonamide

[0249] A 100 mg (0.04 mmol) portion of the4-(4-formyl-3-methoxy-phenoxy) butyramide resin (see step 1 of EXAMPLE20) was suspended in CICH₂CH₂CI (1 mL) and a solution of1-amino-2-(4-bromophenyl)-pent-5-ene (0.048 g, 0.2 mmol, 5 eq) inCICH₂CH₂CI (1 mL) was added. The resin was shaken for 20 min at roomtemperature and then Na(OAc)₃BH (0.045 g, 0.2 mmol, 5 eq) was added. Thereaction was shaken at room temperature for 16 h. The solution wasfiltered and the resin was washed with MeOH (1×), DMF (3×), MeOH (3×)and CH₂CI₂ (3×).

[0250] An aliquot of the resin tested positive with chloranil andnegative with 2,4-dinitrophenylhydrazine.

[0251] The resin was suspended in CH₂CI₂ (3.0 mL) and DIEA (0.035 mL,0.2 mmol, eq) was added followed by 3,5-dichloro-phenyl isocyanate(0.283g, 1.5 mmol, to give a 0.5 M solution). The resin was shaken atroom temperature for 16 h, the solution filtered and the resin washedwith CH₂CI₂ (3×), DMF (3×), MeOH (2×) and CH₂CI₂ (3×). An aliquot of theresin gave a negative chloranil test.

[0252] The resin was added 3-cyanophenylboronic acid (0.024 g, 0.16mmol, 4 eq), K₂CO₃ (0.028 m, 0.2 mmol, 5 eq) and Pd(PPh₃)₄ (0.009 g,0.008 mmol, 0.2 eq). DMF (2 mL, degassed with Ar) was added and themixture was heated to 70° C. for 16 h. The solution was filtered and theresin washed with DMF (4×), H₂O (4×), MeOH (3×) and CH₂CI₂ (4×).

[0253] The resin was shaken at room temperature for 14 h with a solutionof OsO₄ (4% in H₂O, 0.052 mL, 0.008 mmol, 0.2 eq) and NMMO (0.05 g, 0.4mmol, 10 eq) in acetone-H₂O (1:1, 3 mL) at room temperature for 14 h.The solution was filtered and the resin was washed with H₂O (2×),acetone (2×), pyridine (1×, shake for 30 min), MeOH (2×) and CH₂CI₂(3×). A solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) in acetone-H₂O(1:1, 3 mL) was added and the mixture shaken for 2 h. The solution wasfiltered and the resin was washed with H₂O (2×), acetone (1×). The resinwas treated with a fresh solution of NaIO₄ (0.085 g, 0.4 mmol, 10 eq) inacetone-H₂O (1:1, 3 mL) and shaken for a further 2 h. The solution wasfiltered and the resin was washed with H₂O (3×), acetone (1×), MeOH (2×)and CH₂CI₂ (3×).

[0254] The resin was shaken with a solution of piperidin4-yl-carbamicacid tert butyl ester (0.043 g, 0.2 mmol, 5 eq) in CICH₂CH₂CI (1.5 mL)for 30 min. Na(OAc)₃BH (0.05 g, 0.2 mmol, 5 eq) was added and themixture shaken at room temperature for 14 h. The solution was filteredand the resin washed with MeOH (2×), DMF (3×), MeOH (3×) and CH₂CI₂(3×).

[0255] The resin was suspended in CH₂CI₂ (3 mL) and treated with2,6lutidine (0.52 mL, 4.5 mmol, 1.5M final concentration) and TMSOTf(0.54 mL, 3 mmol, 1 M final concentration). The mixture was shaken atroom temperature for 1 h. The solution was filtered and the resin waswashed with CH₂CI₂ (3×), MeOH (3×) and CH₂CI₂ (3×). An aliquot of theresin gave a positive ninhydrin test.

[0256] The resin was suspended in pyridine (1.5 mL) and treated withmethanesulfonyl chloride (1.5 mL of a 1.0M solution in CH₂CI₂). Themixture was is shaken at room temperature for 14 h. The solution wasfiltered and the resin was washed DMF (3×), MeOH (3×) and CH₂CI₂ (3×).

[0257] The resin was treated with a solution of TFA (25% in CH₂CI₂, 3mL) and shaken for 2 h at room temperature, filtered off and thefiltrate was purified by Gilson 215 HPLC (10-90% acetonitrile/water) toyield the title compound (0.0012 g, 5%). MS (ESI): 614.1 (M+1),616.1(M+3).

EXAMPLE 30(R,S)-N-(3,5-Bistrifluoromethylbenzyl)-4-(cyclohexylmethylamino)-2-(3,4-dichloro-phenyl)-butyramide

[0258]

[0259] A 100 mg (0.04 mmol) portion of the4-(4-formyl-3-methoxy-phenoxy) butyramide resin (see step 1 of EXAMPLE20) was suspended in CICH₂CH₂CI (1 mL) and a solution of3,5bistrifluoromethylbenzyl amine (0.05 g, 0.2 mmol, 5 eq) in CICH₂CH₂CI(1 mL) was added. The resin was shaken for 20 min at room temperatureand then NaBH(OAc)₃ (0.045 g, 0.2 mmol, 5 eq) was added. The mixture wasshaken at room temperature for 16 h. The solution was filtered and theresin was washed with MeOH (1×), DMF (3×), MeOH (3×) and CH₂CI₂ (3×). Analiquot of the resin tested positive with chloranil and negative with2,4-dinitrophenylhydrazine.

[0260] The resin was suspended in pyridine (1 mL) and a solution of2-(3,4-dichloro-phenyl)-pent-4-enoyl chloride (0.054 g, 0.2 mmol, 5 eq)in CH₂CI₂ (1 mL) was added. The resin was shaken at room temperature for16 h. The solution was filtered and the resin was washed with MeOH (3×),DMF (3×), MeOH (3×) and CH₂CI₂ (3×). This procedure was repeated usingthe same reaction and washing conditions. An aliquot of the resin gave anegative bead test with chloranil. The resin was shaken at roomtemperature for 14 h with a solution of OsO₄ (4% in H₂O, 0.052 mL, 0.008mmol, 0.2 eq) and NMMO (0.05 g, 0.4 mmol, 10 eq) in acetone H₂O (1:1, 3mL) at room temperature for 14 h. The solution was filtered and theresin was washed with H₂O (2×), acetone (2×), pyridine (1×, shake for 30min), MeOH (2×) and CH₂CI₂ (3×). A solution of NaIO₄ (0.085 g, 0.4 mmol,10 eq) in acetone-H₂O (1:1, 3 mL) was added and the mixture shaken for 2h. The solution was filtered and the resin was washed with H₂O (2×),acetone (1×). The resin was treated with a fresh solution of NaIO₄(0.085 g, 0.4 mmol, 10 eq) in acetone-H₂O (1:1, 3 mL) and shaken for afurther 2 h. The solution was filtered and the resin was washed with H₂O(3×), acetone (1×), MeOH (2×) and CH₂CI₂ (3×).

[0261] The resin was shaken with a solution of N-methylcyclohexylamine0.026 mL, 0.2 mmol, 5 eq) in CICH₂CH₂CI (1.5 mL) for 30 min. Na(OAc)₃BH(0.05 g, 0.2 mmol, 5 eq) was added and the mixture shaken at roomtemperature for 14 h. The solution was filtered and the resin washedwith MeOH (2×), DMF (3×), MeOH (3×) and CH₂CI₂ (3×). An aliquot of theresin gave a positive chloranil test. The resin was treated with asolution of TFA (25% in CH₂CI₂, 3 mL) and shaken for 2 h at roomtemperature, filtered off and the filtrate was concentrated and purifiedby Gilson 215 HPLC (10-90% acetonitrile/water) to yield the titlecompound (0.0039 g, 15%). MS(ESI): 569.1 (M+1), 571.2 (M+3).

EXAMPLE 312-(3′-Cyano-biphenyl-4-yl)-N-(3,5-dichloro-phenyl)-4methylamino-butyramide

[0262]

[0263] To a solution of 4-bromophenylpent-4enoyl chloride (1.0 g, 3.7mmol, EXAMPLE 18) in CH₂CI₂ (15 mL) was added 3,5-dichloroaniline (0.74g, 4.5 mmol, 1.2 eq) and Et₃N (1.5 mL, 11.1 mmol, 3 eq). The reactionmixture was stirred at r.t. for 16 h. The mixture was washed with 10%NaHCO₃ (10 mL), H₂O (10 mL), 1 N HCI (10 mL) and saturated brine, dried(Na₂SO₄), and concentrated. Chromatography on silica gel (10%EtOAc/hexanes) gave 2-(4-bromophenyl)-pent-4-enoic acid(3,5-dichloro-phenyl)amide as a yellow oil (1.5 g, 100%). ¹H NMR (300MHz, CDCI₃): δ 7.62 (d, 2H), 7.53 (d, 2H), 7.33 (d, 2H), 7.19 (t, 1H),5.83 (m, 1H), 5.17 (m, 2H), 3.62 (t, 1H), 3.03 (m, 1H), 2.65 (m, 1H).

[0264] To an Argon-purged solution of 2-(4-bromophenyl)-pent-4-enoicacid (3,5dichloro-phenyl)amide (1.5 g, 3.7 mmol) in toluene/EtOH (2:1v/v, 30 mL) was added 3-cyanophenylboronic acid (0.99 g, 6.7 mmol, 1.8eq), Pd(PPh₃)₄ (160 mg, 0.44 mmol, 12%), and a solution of Na₂CO₃ (2.12g, 20 mmol, 5.4 eq) in 10 mL of water. The reaction mixture was heatedat 90° C. for 16 h. The mixture was partitioned between EtOAc (50 mL)and 10% NaHCO₃ (50 mL) and the organic phase separated. The organicphase was washed with 10% NaHCO₃ (30 mL) and saturated brine (30 mL),dried (Na₂SO₄), and concentrated. Chromatography on silica gel (20%EtOAc/hexanes) gave 2-(3′-cyano-biphenyl-4-yl)-pent-4-enoic acid(3,5-dichloro-phenyl)amide as a yellow oil (685 mg, 44%). ¹H NMR (300MHz, CD₃OD): δ 7.93 (m, 2H), 7.81(m, 2H), 7.66 (m, 4H), 7.49 (m, 2H),7.12 (t, 1H), 5.89 (m, 1H), 5.21(m, 2H). 3.76 (t, 1H), 3.11(m, 1H), 2.73(m, 1H).

[0265] To a solution of 2-(3′-cyano-biphenyl-4-yl)-pent-4-enoic acid(3,5-dichloro phenyl)amide (680 mg, 1.6 mmol) in 9 mL of acetone/H₂O(2:1 v/v) was added OsO₄ (4% in H₂O, 100 L, 1 mmol %) and NaIO₄ (860 mg,4.0 mmol, 2.5 eq). The reaction mixture was stirred at r.t. for 6 h. Themixture was then partitioned between CH₂CI₂ (20 mL) and 10% NaHCO₃ (20mL) and the organic layer separated. The aqueous layer was extractedwith CH₂CI₂ (10 mL×3) and the combined organic layer was washed withsaturated brine (10 mL), dried (Na₂SO₄), and concentrated.Chromatography on silica gel (20% EtOAc/hexanes) gave2-(3′-cyano-biphenyl-4-yl)N(3,5-dichloro-phenyl)-4oxobutyramide as alight yellow oil (300 mg, 44%). MS(ESI): 423.0 (M+1).

[0266] A mixture of2-(3′-cyano-biphenyl-4-yl)N(3,5-dichloro-phenyl)-4oxo-butyramide (300mg, 0.71 mmol) and MeNH₂ (2M in THF, 1.77 mL, 3.54 mmol, 5 eq) in1,2-dichloroethane (3.5 mL) was stirred at r.t. for 1 h and thenNa(AcO)₃BH (299 mg, 1.4 mmol, 2 eq) was added. The reaction mixture wasstirred at r.t. for 16 h. The mixture was then partitioned between EtOAc(20 mL) and 10% NaHCO₃ (10 mL) and the organic phase separated. Theorganic phase was washed with 10% NaHCO₃ (10 mL×2), saturated brine (10mL), dried (Na₂SO₄), and concentrated. Chromatography on silica gel(Et₃N/MeOH/CH₂CI₂ 1:10:90) gave 56.5 mg (18%) of the title compound as ayellowish gum. ¹H NMR (300 MHz, CDCI₃): δ 7.89 ( m, 2H), 7.72 (m, 1H),7.61 (m, 7H), 7.14 (t, 1H), 4.04 (dd, 1H), 2.85 (t, 2H), 2.59 (s, 3H),2.50 (m, 1H), 2.16 (m, 1H). MS(ESI): 438.0 (M+1), 440.0 (M+3).

EXAMPLE 324-{1-[3-(3,5-Dichlorophemyl)-2-oxoimidazolidin-1-ylmethyl]-3-dimethylaminopropyl}biphenyl-3carbonitrile

[0267]

[0268] A solution of 3,5-dichloro-phenyl isocyanate (5 g, 26.6 mmol) intBuOH (100 mL) was heated at 80° C. for 16 h. The mixture wasconcentrated by rotary evaporation to give a white solid which wastriturated with toluene and evaporated to dryness. Addition of tolueneand concentration under vacuum gave (3,5-dichloro-phenyl)carbamicacidtert-butyl ester as a white solid (6 g, 22.9 mmol, 84%). ¹H NMR (300MHz, CDCI₃): δ 7.42 (s, 2H), 7.18 (s, 1H), 6.6 (br s, NH), 1.62 (s, 9H).

[0269] To a solution of (3,5-dichloro-phenyl)carbamic acidtert-butylester (6 g, 22.89 mmol) in DMF (130 mL) at 0° C. under Ar was added NaH(60% dispersion in mineral oil, 1.725 g, 45 mmol, 2 eq). The mixture wasstirred at 0° C. for 30 min and then allyl iodide (13.32 mL, 110 mmol, 5eq) was added over 5 min. The mixture was warmed to room temperature andstirred for 2 h. The mixture was then diluted with EtOAc (200 mL) andwashed with saturated aqueous NaHCO₃ (200 mL). The aqueous phase waswashed with EtOAc (3×60 mL) and the combined organic extracts werewashed with saturated aqueous NaCl (200 mL), dried over Na₂SO₄, filteredand concentrated to give a brown oil which was purified by flash columnchromatography eluting with 2% EtOAc/hexanes to giveallyl(3,5-dichloro-phenyl) carbamic acidtert-butyl ester as a clear oil(4.632 g, 15.33 mmol, 67%).). ¹H NMR (300 MHz, CDCI₃): δ 7.41 (s, 1H),7.24 (m, 2H), 6.00 (m, 1H), 5.30 (m, 2H), 4.30 (m, 2H), 1.59 (s, 9H).

[0270] A stirred solution of allyl(3,5-dichloro-phenyl)carbamicacidtert-butyl ester (2.32 g, 7.68 mmol) in CH₂CI₂ (75 mL) was cooled to−78° C. Ozone was bubbled through for ˜5 min (reaction monitored bytic). Oxygen was then bubbled through for 5 min. Me₂S (5 mL, 77 mmol, 10eq) was added and the mixture was warmed to room temperature and stirredfor 6 h. Following a further addition of Me₂S (5 mL, 77 mmol, 10 eq) themixture was stirred at room temperature for 14 h. The mixture wasconcentrated by rotary evaporation and the resulting residue waspurified by flash column chromatography eluting with 25% EtOAc/hexanesto yield (3,5-dichloro-phenyl)(2oxoethyl)carbamic acidtert-butyl ester(1.61 g, 5.3 mmol, 69%) as a pale oil. ¹H NMR (300 MHz, CDCI₃): δ 9.80(s, 1H), 7.30 (m, 3H), 4.45 (s, 2H), 1.56 (s, 9H).

[0271] To a stirred solution of (3,5-dichloro-phenyl)(2oxoethyl)carbamicacid-tert-butyl ester (0.75 g, 2.46 mmol) in MeOH (15 mL) under Ar atroom temperature was added a solution of (R,S)2-(4iodophenyl)-pent-4enylamine (0.741 g, 2.58 mmol, 1.05 eq) in MeOH (5mL). The mixture was stirred at room temperature for 5 h. NaBH₄ (0.140g, 3.69 mmol, 1.5 eq) was added and the resulting mixture was stirredfor a further 1 h, quenched by the addition of NaOH (1 M aqueoussolution, 20 mL). The mixture was extracted twice with Et₂O (50 mLtotal) and the combined organic extracts were washed with saturatedaqueous NaCI and dried over Na₂SO₄. Filtration and concentration of thefiltrate by rotary evaporation gave the crude product which was purifiedby flash column chromatography eluting 12% EtOAc/hexanes to give(3,5-Dichloro-phenyl){-2-[2-(4-iodophenyl)-pent-4-enylamino]ethyl}carbamicacid tert-butyl ester (0.493 g, 0.85 mmol, 35%) as a pale oil. ¹H NMR(300 MHz, CDCI₃): δ 7.75 (d, 2H), 7.29 (td,2H), 7.18 (d, 2H), 7.04 (d,2H), 5.74 (m,1H), 5.06 (m, 2H), 3.74 (td, 2H), 2.82 (m, 5H), 2.44 (m,2H), 1.52 (s, 9H).

[0272] To a stirred solution of(3,5-dichloro-phenyl){2-[2-(4-iodophenyl)-pent-4-enylamino]ethyl}carbamicacid tert-butyl ester (0.493 g, 0.85 mmol) in CH₂CI₂ (20 mL) at 0° C.was added TFA (5 mL). The mixture was stirred and warmed to roomtemperature for 4 h. The solvent was removed by rotary evaporation andthe residue was dissolved in EtOAc and washed twice with NaHCO₃ (10% inH₂O). The organic extracts were dried over sodium sulfate, filtered andconcentrated by rotary evaporation to giveN(3,5-dichloro-phenyl)N′[2-(4iodophenyl)-pent-4-enyl]ethane1,2diamine(0.386 g, 0.81 mmol, 95%) as a brown oil. ¹H NMR (300 MHz, CDCI₃): δ7.73 (d, 2H), 7.03 (d, 2H), 6.56 (t, 1H), 6.50 (d, 2H), 5.75 (m, 1H),5.08 (m, 2H), 4.42 (br s, NH), 3.15 (m, 2H), 3.40 (m, 5H), 2.44 (m, 2H).

[0273] To a stirred solution ofN(3,5-dichloro-phenyl)N′[2-(4iodophenyl)-pent-4-enyl]ethane1,2diamine(0.386 g, 0.81 mmol) in toluene (10 mL) was added CDI (0.18 g, 1.1 mmol,1.4 eq). The mixture was heated to 100° C. for 16 h, then cooled to roomtemperature, diluted with EtOAc (25 mL) and washed twice with saturatedaqueous NaCl (25 mL). The organic extracts were dried over sodiumsulfate, filtered and concentrated by rotary evaporation to give a darkbrown oil. The crude product was purified by flash column chromatographyeluting with 10% EtOAc/hexanes to give 1(3,5-dichloro-phenyl)-3-[2-(4-iodophenyl )-pent-4-enyl]-imidazolidin2one (0.128 g, 0.255mmol, 30%) as a pale foam. ¹H NMR (300 MHz, CDCI₃): δ 7.74 (d, 2H), 7.54(d, 2H), 7.20 (m, 3H), 5.75 (m, 1H), 5.10 (m, 2H), 3.74 (m, 3H), 3.38(m, 2H), 3.22 (m, 1H), 3.08 (m, 1H), 2.50 (m, 2H).

[0274] A solution of1-(3,5-dichloro-phenyl)-3-[2-(4iodophenyl)-pent-4enyl]-imidazolidin-2-one(0.128 g, 0.255 mmol), 3-cyanophenyl boronic acid (0.113 g, 0.766 mmol,3 eq), tris(dibenzylidene-acetone)-dipalladium(O) (0.025g, 0.0255 mmol,10 mol %), triphenylarsine (0.031 g, 0.1 mmol, 40 mol %) and cesiumfluoride (0.075 g, 0.51 mmol, 2 eq) in DME (13 mL) and ethanol (3 mL)was microwaved at 50W for 7 h and then at 100W for 1 h. The mixture wasdiluted with EtOAc (50 mL), filtered through a pad of celite 545® andthe filtrate washed with saturated aqueous Na₂CO₃ solution (25 mL). Theaqueous layer was extracted twice with EtOAc (50 mL). The combinedorganic extracts were washed with saturated aqueous Na₂CO₃ solution (25mL) and saturated aqueous sodium chloride solution (25 mL). The organiclayer was separated, dried over sodium sulfate, filtered andconcentrated to give a dark oil. Purification by flash columnchromatography eluting 1520% EtOAc/hexanes gave4′-{1-[3-(3,5-dichloro-phenyl)-2-oxo-imidazolidin1-yl-methyl]but-3enyl}biphenyl-3carbonitrile(0.059 g, 0.125 mmol, 49%) as a dark foam. ¹H NMR (300 MHz, CDCI₃): δ7.98 (m, 1H), 7.92 (m, 1H), 7.74 (m, 1H), 7.64 (m, 3H), 7.58 (d, 2H),7.45 (d, 2H), 7.11 (dd, 1H), 5.80 (m, 1H), 5.12 (m, 2H), 3.75 (m, 3H),3.55 (m, 1H), 4.42 (m, 1H), 3.26 (m, 2H), 2.58 (dd, 2H).

[0275] Ozone was bubbled through a solution of4′-{1-[3-(3,5-dichloro-phenyl)-2-oxoimidazolidin1-ylmethyl]but-3-enyl}biphenyl-3carbonitrile(0.059g, 0.124 mmol) in CH₂CI₂ (15 mL) at −78° C. After 5 min, oxygenwas bubbled through followed by the addition of DMS (0.1 mL, 12.5 mmol,10 eq). The mixture was warmed to room temperature and stirred for 18 h.The solvent was removed by rotary evaporation and the resulting residuewas dissolved in CICH₂CH₂CI (2 mL) and dimethylamine (2M in THF, 0.06mL, 0.12 mmol, 1 eq) was added. The mixture was stirred at roomtemperature for 1 h and then Na(OAc)₃BH (0.033 g, 0.16 mmol, 1.3 eq) wasadded. The mixture was stirred at room temperature for 16 h and thenpartitioned between saturated aqueous NaHCO₃ (10 mL) and EtOAc (20 mL).The organic layer was washed with saturated aqueous NaCI, dried overNa₂SO₄, filtered and concentrated to yield the crude product.Purification by HPLC gave the title compound4′-{1-[3-(3,5-dichlorophemyl)-2oxoimidazolidin-1-ylmethyl]3-dimethylaminopropyl}biphenyl-3carbonitrile(0.016 g, 0.02 mmol, 16%) as a pale yellow oil. ¹H NMR (300 MHz, CDCI₃):δ 7.96 (m, 1H), 7.92 (dt, 1H), 7.76 (dt, 1H), 7.68 (m, 3H), 7.56 (d,2H), 7.46 (d, 2H), 7.14 (t, 1H), 3.82 (m, 3H), 3.44 (m, 3H), 3.4 (m,2H), 2.94 (br s, 6H), 2.30 (m, 2H); MS(ESI): 507.1 (M+1), 509.0 (M+3).

EXAMPLE 33 (3,5-Dichloro-phenyl)carbamic acid3dimethylamino-1(4-pyridin4-yl phenyl)propyl ester

[0276]

[0277] A mixture of 2-(4iodophenyl)-pent-4-enenitrile (2.8 g, 9.9 mmol,intermediate for preparing EXAMPLE 2), OsO₄ (0.7 mL, 4% in water, 0.10mmol), and NaIO₄ (4.44 g, 20.8 mmol) in 2:1 acetone/H₂O (100 mL) wasstirred at room temperature for 16 h. TLC (1:1 hexanes/EtOAc) showed nostarting material left. The mixture was diluted with H₂O (50 mL) andextracted with CH₂CI₂ (50 mL×4). The organic layer was washed withbrine, dried (Na₂SO₄) and concentrated by rotary evaporation.Purification by silica gel chromatography (1:1 hexanes/EtOAc) gave2-(4iodophenyl)-4oxobutyronitrile as a yellowish oil, 1.9 g (68%). ¹HNMR (300 MHz, CDCI₃): δ 9.85 (s,1H), 7.84 (d, 2H), 7.24 (d, 2H), 4.44 (t,1H), 3.33 (dd, 1H), 3.14 (dd, 1H).

[0278] To a solution of 2-(4iodophenyl)-4oxobutyronitrile (2.03 g, 7.1mmol) in CICH₂CH₂CI (50 mL) was added dimethylamine (14.3 mL, 2M in THF,28.6 mmol, 4 eq) and the mixture was left stirring at room temperaturefor 1 h. Na(OAc)₃BH (6.04 g, 28.6 mmol, 4 eq) was added and the mixturewas stirred at room temperature for 16 h. The reaction was quenched byadding aqueous saturated NaHCO₃ (50 mL) and the mixture was extractedwith EtOAc (50 mL×3). The organic layer was washed with saturatedaqueous NaCI, dried over Na₂SO₄ and concentrated. The crude product waspurified by silica gel chromatography (50% EtOAc/hexanes) to give4dimethylamino-2-(4iodophenyl)-butyronitrile as a dark brown solid, 2.09g (94%). ¹H NMR (300 MHz, CDCI₃): δ 7.83 (d, 2H), 7.22 (d, 2H), 4.10 (t,1H), 2.56 (m, 1H), 2.41 (m, 1H), 2.34 (s, 6H), 2.20 (m, 1H), 2.05 (m,1H).

[0279] To a solution of 4dimethylamino-2-(4iodophenyl)-butyronitrile(1.02 g, 3.2 mmol) in 2:1 toluene/EtOH (30 mL) was added 2M Na₂CO₃ (10mL, 20 mmol), pyridine4boronic acid pinacol cyclic ester (1.0 g, 4.9mmol), and Pd(PPh₃)₄ (116 mg, 0.31 mmol). The resulting mixture washeated at 90° C. under Ar for 16 h. TLC (10% MeOH/CH₂CI₂) showed nostarting material left. The mixture was diluted with EtOAc (100 mL),washed with saturated aqueous NaHCO₃ (50 mL×3), saturated aqueous NaCI(50 mL×3), dried over Na₂SO₄ and concentrated by rotary evaporation. Thecrude residue was purified using silica gel chromatography (2-10%MeOH/CH₂CI₂ gradient) to give 4dimethylamino-2-(4-pyridin4-ylphenyl)butyronitrile as a brown oil, 680 mg (80%). ¹H NMR (300 MHz, CDCI₃): δ8.79 (dd, 2H), 7.78 (d, 2H), 7.60 (m, 4H), 4.22 (dd, 1H), 2.61 (m, 1H),2.46 (m, 1H), 2.37 (s, 6H), 2.24 (m, 1H), 2.15 (m, 1H).

[0280] To a solution of4dimethylamino-2-(4-pyridin4-ylphenyl)-butyronitrile (680 mg, 2.56 mmol)in THF (5 mL) was added LiAIH₄ (1 M in THF, 26 mL, 26 mmol) and themixture was stirred at room temperature for 16 h. TLC (10% MeOH/CH₂CI₂)showed no starting material left and a new low Rf spot was formed. Themixture was treated with 1.74 mL of H₂O, followed by 3.48 mL of 1 Naqueous NaOH, and then 5.2 mL of H₂O. After 30 min of stirring, themixture was filtered and the filtrate was dried over Na₂SO₄ andconcentrated to give 3dimethylamino-1-(4pyridin4-ylphenyl)propan1ol as ayellowish solid, 300 mg (46%). ¹H NMR (300 MHz, CDCI₃): δ 8.75 (dd, 2H),7.74 (m, 2H), 7.62 (m, 4H), 5.12 (dd, 1H), 2.82 (m,1H), 2.64 (m, 1H),2.44 (s, 6H), 1.97 (m, 2H).

[0281] To a solution of 3dimethylamino-1(4-pyridin4-ylphenyl)propan1ol(100 mg, 0.37 mmol) in CH₂CI₂ (2 mL) was added3,5-dichloro-phenylisocyanate (70 mg, 0.37 mmol) and the mixture wasstirred at room temperature for 16 h. The mixture was concentrated togive a light brown oil, which was then purified by silica gelchromatography (5-10% MeOH/DCM gradient) to afford the title compound(3,5-dichloro-phenyl)carbamic acid3-dimethylamino-1-(4-pyridin4-ylphenyl)propyl ester as a white solid,131 mg (91%). ¹H NMR (300 MHz, CD₃OD): δ 8.77 (dd, 2H), 7.72 (d, 2H),7.58 (m, 3H), 7.48 (d, 2H), 7.12 (t, 1H), 5.94 (t, 1H), 2.49 (m, 2H).2.36 (s, 6H), 2.33 (m, 1H), 2.21 (m, 1H); MS(ESI): 444.1 (M+1), 446.1(M+3).

[0282] Table I provides additional Examples (#34-457) of MCH activecompounds that were prepared using the methods as described for Examples20-33.

[0283] MCH Assay PCOP Protocol

[0284] A reaction mixture of 10 μg hMCHR-CHO overexpressing membranes(from Receptor Biology, Inc., Beltsville, Md., or internally produced)and 100 -μg/well WGA-SPA beads (from Amersham Pharmacia Biotech, Inc.,Piscataway, N.J.)/100 μl was prepared in MCHR assay buffer (25 mM HEPES,pH 7.4, 10 mM NaCI, 10 mM MgCI₂, 5 mM MnCI₂, 0.1%BSA). A 2.0 nM stock ofligand, [¹²⁵I]-MCH (from Perkin Elmer Life Sciences, Inc., Boston,Mass.) was prepared in the MCHR assay buffer. 40×stock solutions of testcompounds were prepared in DMSO and then added to a 96well assay plate(Corning #3604, Corning, N.Y.) as follows: 5 μl test compound, testcompound or DMSO, 45 μl MCHR assay buffer, 100 -μl of reaction mixture,50 μl of ligand stock (Final [Ligand]=0.5 nM). The assay plates wereshaken for 5 minutes on a plate shaker, then incubated for 2 hoursbefore cpm/well were determined in a Microbeta Trilux counter (fromPerkinElmer Wallac, Inc., Gaithersburg, Md.). Percent inhibition oftotal bindingnonspecific binding (2.5 -μM MCH) was determined for IC₅₀values. TABLE I MCH Antagonist Compounds- A: Ki = 0.4-50 nM; B: ki =51-500 nM; C: Ki = 501-2,500 nM Exact MS, MS (ESI) Example Chemistrycalc. found Activity 20

540.1169 541.1, 543.1 C 21

508.0312 509.1, 511.0, 513.0 C 22

468.1131 469.0, 471.0 C 23

520.1796 521.0, 523.0 C 24

419.1809 420.1, 421.1 C 25

501.1044 502.1, 504.1 C 26

461.1870 462.2 C 27

592.2120 593.1, 595.1 C 28

693.1231 693.9, 695.9, 697.9 C 29

613.1681 614.1, 616.1 C 30

568.1482 569.1, 571.2 C 31

437.1061 438.0, 440.0 C 32

506.1640 507.1, 509.0 C 33

443.1167 444.1, 446.1 C 34

496.1796 497.1, 499.1 A 35

513.2062 514.1, 516.0 A 36

456.1483 457.2, 459.2 A 37

512.1745 513.2, 515.3 A 38

498.1589 499.2, 501.1 A 39

456.1483 457.2, 459.2 B 40

488.1382 489.1, 491.1 C 41

488.1382 489.1, 491.1 C 42

443.1167 444.1, 446.1 C 43

458.1873 459.0, 461.1 A 44

434.1918 435.0, 436.1 A 45

432.1717 432.9, 435.0 A 46

450.1622 451.0, 453.0 A 47

448.2074 449.1, 450.2 A 48

448.2074 449.1, 450.0 A 49

416.2012 417.0, 418.1 A 50

464.1779 465.0 A 51

446.1873 447.1, 449.1 A 52

430.2169 431.1, 432.1 A 53

460.2074 461.0, 462.1 A 54

442.2169 443.1 A 55

412.2263 413.1, 414.1 A 56

476.1779 477.0, 479.1 A 57

398.2106 399.0, 400.0 A 58

424.2263 425.0, 426.2 A 59

442.2169 443.0, 444.1 A 60

416.2012 417.0, 418.1 A 61

430.2169 431.1, 432.1 A 62

446.1873 447.1, 449.1 A 63

442.2369 443.1 A 64

432.1717 433.0, 434.0 A 65

458.1873 459.1, 461.0 A 66

433.1965 434.1, 335.2 A 67

433.1965 434.1, 435.1 B 68

445.1965 446.1, 447.1 B 69

445.1965 446.1, 447.1 B 70

419.1809 420.1, 421.1 B 71

413.2215 414.0 B 72

510.1589 511.1, 513.0 A 73

466.1327 467.4, 469.1 A 74

488.2387 489.1, 490.1 A 75

504.2092 505.1, 507.1 A 76

492.1483 493.0, 494.0, 495.0, 496.0 A 77

480.1483 481.0, 483.0 A 78

480.1483 481.1, 483.1 A 79

520.1796 521.1, 523.1 A 80

494.1640 495.0, 497.1 A 81

522.1589 523.1, 525.1 A 82

505.1687 506.1, 508.1 B 83

473.2278 474.1, 475.2 B 84

455.2373 456.1, 457.2 B 85

471.2077 472.1, 473.1 B 86

558.1259 558.9, 560.8 B 87

598.1572 598.9, 601.0 C 88

596.1932 597.1, 599.0 A 89

579.1667 579.9, 582.1 A 90

531.1655 532.0, 534.1 A 91

513.1750 514.1, 516.0 A 92

548.1921 549.0, 551.1 A 93

520.1796 521.0, 523.1 A 94

512.1745 513.0, 515.1 A 95

531.1655 532.0, 534.1 A 96

496.1796 497.3, 499.3 B 97

514.1902 515.0, 517.3 B 98

537.2062 538.1, 540.1 B 99

548.1921 549.0, 551.1 B 100

531.1655 532.0, 534.0 B 101

596.1932 597.0, 599.2 B 102

548.1921 549.0, 551.1 C 103

447.1844 448.1, 450.1 B 104

474.1670 475.1, 477.0 B 105

512.1148 513.0, 515.1, 517.1 B 106

463.1429 464.1, 466.0 B 107

501.0908 502.0, 503.9, 505.1 B 108

521.1668 522.1, 523.0 B 109

515.2371 516.1 B 110

436.1336 437.0, 439.0 B 111

518.1173 518.9, 520.9, 523.0 B 112

470.1407 470.9, 472.9 C 113

496.1444 497.0, 499.0 C 114

469.1499 470.0, 472.1 C 115

529.1414 530.0, 532.1 C 116

480.1695 481.0, 483.0 C 117

513.1709 514.0, 516.0 C 118

464.2109 465.1, 467.0 C 119

486.1764 487.1, 489.0 C 120

491.1935 492.1 C 121

458.1965 459.1 C 122

540.1461 541.0, 543.0, 545.1 B 123

520.2008 521.1, 523.0 B 124

453.1141 454.0, 456.0 B 125

594.1448 594.8, 596.8, 597.9 B 126

583.1207 583.8, 585.8, 587.1 B 127

433.1687 434.1, 436.1, 438.0 B 128

540.2115 541.0, 543.1, 544.1 B 129

599.0912 599.8, 601.8, 603.8 B 130

453.1141 454.0, 455.9, 458.0 B 131

567.1503 567.8, 569.9, 570.9 B 132

599.1565 599.8, 601.9, 602.9 B 133

497.0636 497.9, 499.9, 502.0 B 134

471.1047 472.0, 475.0, 476.0 B 135

488.0704 488.9, 490.9, 493.0 B 136

463.1025 464.0, 466.0, 468.1 B 137

520.2661 521.1, 522.2 B 138

534.1236 535.0, 537.0 B 139

419.1531 420.0, 421.9, 423.1 C 140

507.1292 508.0, 510.0, 511.1 C 141

482.1287 483.0, 485.0 C 142

399.2077 400.0, 402.1 C 143

443.1572 444.1, 447.0 C 144

455.1342 456.0, 458.0 C 145

434.1640 435.0, 437.0 C 146

642.1599 643.0 B 147

539.1742 540.1, 542.0 B 148

540.1695 541.0, 543.2 B 149

520.1796 521.0, 523.1 B 150

580.1983 581.1, 583.0 B 151

546.1720 547.0, 549.0 B 152

529.1454 530.0, 532.0 B 153

585.2161 586.0, 588.0 B 154

542.2215 543.1, 545.1 B 155

513.1750 514.1, 516.0 B 156

513.1750 514.0, 516.1 B 157

563.1064 564.1, 566.0, 568.0 B 158

529.1454 530.0, 532.0 B 159

547.1360 548.0, 550.1 B 160

459.1844 460.1, 462.2 B 161

509.2000 510.0, 512.1, 514.1 C 162

526.2266 527.0, 529.1 C 163

556.2008 557.1, 559.1 C 164

525.1950 526.1, 528.1 C 165

530.2015 531.0, 533.1 C 166

529.1454 530.0, 532.0 C 167

580.1330 581.0, 582.9, 585.0 C 168

569.2324 570.1, 572.2 C 169

537.2062 538.1, 540.1 C 170

564.1625 565.0, 567.0 C 171

512.2109 513.1, 515.0 C 172

513.2062 514.0, 516.2 C 173

530.2015 531.1, 533.1 C 174

542.2215 543.1, 545.1 C 175

648.1857 649.0, 651.0 C 176

546.1720 547.0, 549.0 C 177

525.1465 525.9, 527.9, 530.0 B 178

536.1512 537.1, 539.1, 541.2 B 179

546.1026 547.1, 551.1 B 180

505.2011 506.0, 508.1 B 181

570.1122 571.0, 573.0, 575.1 B 182

559.1075 559.9, 562.0, 563.9 B 183

564.0920 565.0, 567.0, 569.1 B 184

516.2058 517.1, 519.3 B 185

550.1669 551.0, 553.1 B 186

496.1199 497.1, 501.1 B 187

530.2215 531.1, 533.2 B 188

560.0915 561.0, 563.0, 565.1 B 189

526.1572 527.0, 529.1 B 190

598.0530 598.9, 601.0, 603.0 B 191

584.1279 585.2, 587.1, 589.1 B 192

540.1461 541.0, 543.0 B 193

549.1101 552.0, 554.1 B 194

526.1305 527.1, 529.0 B 195

574.1072 575.1, 577.0, 579.1 B 196

510.1356 511.0, 513.1 B 197

594.1026 597.0, 599.1 B 198

558.1623 559.1, 561.2 B 199

544.0966 545.0, 547.0, 549.0 B 200

628.0636 629.0, 631.0, 632.9 C 201

608.1182 609.1, 611.0 C 202

529.1647 530.1, 532.1 C 203

588.1728 589.0, 591.1 C 204

532.0869 533.0, 535.0 C 205

543.1804 544.1, 546.2 C 206

490.1902 491.1, 493.2 C 207

512.1415 513.0, 515.0 C 208

506.1851 507.1, 509.1 C 209

583.0711 584.0, 586.0, 588.0 C 210

530.0809 531.0, 533.0, 535.0 C 211

566.0479 567.0, 569.0, 571.0 C 212

612.0687 613.2, 615.0 C 213

520.2008 521.1, 523.1 C 214

563.1257 564.0, 566.1, 568.0 C 215

476.1745 477.1, 479.1 C 216

578.1076 579.1, 581.0 C 217

597.0868 598.0, 600.1, 602.2 C 218

537.2062 538.0, 548.1 A 219

540.1695 541.1, 543.0 A 220

557.1960 558.0, 568.1 A 221

546.1720 547.0, 549.0 A 222

529.1454 530.0, 532.1 A 223

556.2008 557.0, 559.0 A 224

564.1625 565.0, 567.0, 569.1 A 225

495.1844 496.1, 498.1 A 226

547.1360 548.1, 550.0, 552.0 B 227

539.1742 540.0, 542.0 B 228

585.2161 586.2, 588.1 B 229

501.1408 502.1, 504.0 B 230

501.1408 502.1, 504.0 B 231

518.1674 519.0, 521.0 B 232

546.1720 547.1, 549.0, 551.0 B 233

512.2109 513.1, 515.1 B 234

529.1454 530.0, 532.1 B 235

518.1674 519.1, 521.0 B 236

563.1064 564.0, 565.9, 568.0 B 237

530.2015 531.0, 533.0 B 238

525.1950 526.1, 528.1 B 239

572.2321 573.1, 575.1 B 240

542.2215 543.1, 545.1 B 241

525.1950 526.0, 528.0 B 242

511.1793 512.0, 514.0 B 243

513.1750 514.1, 516.0 B 244

529.1454 530.0, 532.0, 534.0 B 245

563.1064 564.0, 566.0, 568.0, 570.0 B 246

546.1720 547.0, 549.0 B 247

580.1330 581.0, 583.0, 585.0 B 248

539.1742 540.1, 542.1 B 249

509.2000 510.1, 512.1 B 250

563.1718 564.0, 566.0 B 251

528.2058 529.1, 531.1 B 252

542.2215 543.1, 545.1 B 253

631.1591 632.1, 634.1 C 254

526.2266 527.1, 529.1 C 255

580.1983 581.0, 583.1 C 256

648.1857 649.1, 651.1 C 257

602.2426 603.1, 605.1, 606.1 C 258

552.2234 555.0, 557.0, 558.0, 559.1 B 259

599.0912 597.9, 599.9, 602.0 B 260

558.1367 559.0, 561.0 B 261

537.0789 537.8, 539.9, 541.8 B 262

542.1663 543.0, 545.0 B 263

457.0890 457.9, 459.9, 462.0 C 264

569.1607 570.0, 572.0 C 265

441.1186 442.0, 444.0 C 266

467.1298 468.1, 470.1 B 267

453.1141 454.0, 456.0 B 268

447.1844 448.0, 450.2 B 269

501.2214 502.2 B 270

515.2371 516.1 B 271

433.1687 434.0, 436.1 B 272

419.1531 420.0, 422.1 B 273

439.0985 440.0, 442.0 B 274

487.2058 488.1 B 275

460.1432 460.8, 462.9 C 276

480.0886 480.7, 482.9 C 277

574.1072 575.0, 576.9, 579.0 B 278

539.0701 540.0, 541.9, 544.0 B 279

487.0751 488.0, 490.0, 492.0 B 280

487.0751 487.9, 490.0, 491.9 B 281

574.1725 575.0, 577.0 B 282

473.0595 475.9, 479.1 B 283

473.1248 474.1, 476.1 B 284

527.0813 528.0, 530.0, 531.9 B 285

562.1514 563.0, 565.0 B 286

581.1727 582.1, 584.1, 586.1 B 287

473.0595 474.0, 476.0, 478.0 B 288

489.1561 490.0, 492.0 B 289

489.0908 492.0, 494.1 B 290

487.1405 488.0, 490.1 B 291

516.1017 517.1, 519.0, 521.0 B 292

516.1017 517.0, 519.0, 521.0 B 293

539.1354 540.0, 541.9 B 294

562.0860 563.1, 565.0, 567.0 C 295

553.0493 553.8, 555.8, 557.8 C 296

553.0493 553.9, 555.9 C 297

527.0813 528.0, 530.0, 531.9 C 298

530.1173 530.9, 533.0, 535.0 C 299

473.1248 474.1, 476.0 C 300

530.1827 531.1, 533.1 C 301

530.1173 531.0, 532.9, 535.1 C 302

553.1146 553.9, 555.9 C 303

527.1466 528.1, 530.0 C 304

504.1017 505.0, 506.9 C 305

504.1017 505.0, 507.0, 509.0 C 306

516.1670 517.0, 519.1 C 307

488.0704 489.0, 491.0, 493.1 C 308

488.0704 489.0, 491.0, 493.1 C 309

488.1357 489.0, 491.1 C 310

504.1670 505.1, 507.0 C 311

570.1486 571.0, 573.1, 575.1 B 312

580.1371 581.0, 583.0, 585.0 B 313

536.1876 560.0, 562.0, 564.0 B 314

541.1122 542.8, 544.8 B 315

547.2117 548.1, 550.0, 551.1 B 316

559.1075 560.0, 562.0, 564.1 C 317

547.2117 548.1, 550.1 C 318

556.1231 556.9, 559.1 C 319

621.1020 621.8, 623.8 C 320

630.1387 631.0, 632.9, 634.0 C 321

525.1465 526.0, 528.0 C 322

502.0860 503.0, 505.0, 507.1 C 323

573.1231 574.0, 576.0 C 324

488.1796 449.1, 451.1 C 325

536.1876 537.0, 539.0 C 326

580.1371 581.0, 583.0, 585.0 C 327

519.2167 520.1, 522.1 C 328

555.1278 556.1, 558.1 A 329

507.1512 508.2, 510.2 B 330

596.1777 597.1, 599.1 B 331

592.2272 593.1 B 332

558.1387 559.0, 561.0 B 333

596.1777 597.1, 599.1 B 334

507.1512 508.2, 510.1 C 335

503.2007 504.2 C 336

576.2323 577.1 C 337

538.1934 539.1, 541.1 C 338

487.2058 488.2 C 339

533.1106 534.0, 535.9 C 340

549.0811 549.9, 551.9, 553.0 C 341

491.1807 492.2 C 342

549.0811 552.0, 554.0 C 343

580.2073 581.1 C 344

538.1934 539.1 C 345

534.2429 535.1 C 346

522.2229 523.2 C 347

518.2480 519.2 C 348

584.0625 585.1, 587.1, 589.1, 591.2 C 349

460.0546 461.1, 463.1, 465.1 C 350

433.1687 434.2, 436.2 B 351

516.2422 517.2, 519.1 B 352

433.1687 434.2, 436.2 B 353

433.1687 434.1, 436.1 B 354

425.2678 426.2 C 355

393.2780 394.2 C 356

565.2022 566.1, 568.2 B 357

538.2077 539.1, 541.1 B 358

570.1486 571.1, 573.1, 575.1 C 359

658.0475 659.0, 661.0, 663.0, 665.0 C 360

570.1486 571.1, 573.1, 575.1 C 361

534.2328 535.2, 537.1 C 362

586.2089 587.2, 589.1 C 363

556.1983 557.2, 559.2 C 364

554.1782 555.1, 557.1, 559.1 B 365

570.2140 571.2, 573.2 B 366

570.1486 571.1, 573.2 B 367

595.1340 596.1, 598.1 C 368

570.2140 571.2, 573.1 C 369

538.2077 539.1, 541.1 C 370

562.2477 563.2, 565.1 C 371

556.1231 557.1, 559.1 C 372

591.1047 592.1, 594.1, 596.0 C 373

588.2045 589.1, 591.0, 593.1 C 374

520.2172 521.2, 523.1 C 375

527.2218 528.2, 530.1 C 376

591.1700 592.1, 594.1 C 377

530.2579 531.2, 533.2 C 378

522.2373 523.2, 524.3 C 379

526.1013 527.0, 529.0 C 380

569.1435 570.0, 572.1 C 381

633.1184 634.0, 636.0 C 382

554.1326 555.0, 557.1 C 383

570.1275 571.1, 573.1 C 384

572.1432 573.1, 575.1 C 385

615.1278 616.0, 618.0 C 386

633.1184 634.0, 635.9 C 387

570.1275 571.1, 573.1 C 388

580.1231 581.1, 583.1 C 389

556.1119 557.1, 559.1 C 390

666.1042 667.0, 669.0 C 391

500.1609 501.1, 503.1 C 392

592.1119 593.1, 595.0 B 393

544.0755 545.0, 547.0 C 394

645.1384 645.9, 648.1 C 395

542.1326 543.1, 545.0 C 396

645.1384 646.0, 648.1 C 397

627.1278 628.0, 629.9 C 398

526.1013 527.1, 529.0 C 399

647.1341 648.0, 650.0 C 400

615.1278 616.0, 618.0 C 401

568.1482 569.1, 571.1 C 402

633.1384 634.2, 636.1 C 403

540.1169 541.1, 543.1 C 404

556.1119 557.1, 559.1 C 405

554.1326 555.2, 557.1 C 406

526.1013 527.1, 529.1 C 407

583.1591 584.1, 586.0 C 408

568.1482 569.1, 571.1 C 409

572.1432 573.1, 575.1 C 410

629.1435 630.0, 632.1 C 411

569.1435 570.1, 572.1 C 412

528.1169 529.1, 531.0 C 413

583.1591 584.1, 586.1 C 414

580.1231 581.1, 583.1 C 415

633.1184 634.1, 636.0 C 416

667.2167 668.0, 670.1 C 417

554.1326 555.2, 557.1 C 418

609.1748 610.0, 612.1 C 419

554.1326 555.1, 557.2 C 420

604.1119 605.0, 607.0 C 421

681.1595 681.9, 683.9 B 422

541.1122 542.1, 544.1 B 423

598.1700 599.1, 601.1 B 424

557.1435 558.1, 560.1 C 425

572.1544 573.1, 575.1 C 426

607.1228 608.1, 610.1 C 427

557.1071 558.1, 560.1 C 428

600.1493 601.1, 603.0 C 429

652.2170 653.1, 655.1 C 430

624.1857 625.1, 627.1 C 431

571.1228 572.1, 574.0 C 432

571.1228 572.2, 574.1 C 433

543.1278 544.1, 546.1 C 434

660.1493 661.1, 663.1 C 435

606.1387 607.1, 609.0 C 436

655.0897 656.0, 658.0 C 437

660.1493 661.0, 663.0 C 438

644.1544 645.0, 647.1 C 439

662.1450 663.0, 665.0 C 440

583.1591 584.2, 586.1 C 441

585.1384 586.2, 586.1 C 442

638.2013 639.2, 641.1 B 443

584.2949 585.2 B 444

555.1278 556.2, 558.1 B 445

501.2214 502.2 C 446

472.0642 473.1, 475.1, 477.2 C 447

438.1032 439.1, 441.1, 443.1 C 448

569.1534 570.0, 572.1, 574.0 C 449

472.1296 473.2, 475.1 C 450

418.1578 419.1, 421.1 C 451

515.2470 516.2, 518.1 C 452

555.1377 556.1, 558.2 C 453

429.1374 430.2, 432.1 C 454

486.2105 487.2 C 455

422.1328 423.1, 425.1 C 456

432.1735 433.1, 435.1 C 457

623.1904 624.1 C

What is claimed is:
 1. A compound, including enantiomers, stereoisomers,rotamers, tautomers and prodrug of said compound, and pharmaceuticallyacceptable salts or solvates of said compound or of said prodrug, saidcompound having the general structure shown in Formula I:

wherein: Ar¹=unsubstituted or substituted phenyl, pyridine,pyridine-N-oxide, pyrazine or pyridazine, wherein the substituentsnumber from 0 to 5, may be the same or different and are independentlyselected from the group consisting of H, CN, OCF₃, F, Cl, Br, I, CONH₂,methylenedioxy, OR, CO₂H, CO₂R, and OH with R being a C₁-C₆ straightchain alkyl or branched alkyl or a C₃-C₇ cycloalkyl; M is H or R; Z=

where Ar² is an unsubstituted or substituted phenyl wherein thesubstituents number from 0 to 5, may be the same or different and areindependently selected from the group consisting F, Cl, Br, I, R, OR,NO₂, and CF₃; n=0 to 6; p=1-6; R₁ may be the same or different and isindependently selected from the group consisting of R; NH₂; NHR; N(R)₂;N(R)₂→O; NH(CH₂)_(n)OR; N(R)SO₂R; NH(CH₂)_(n)—N(R)₂; N(R)SO₂(R);

where n is defined above and where Y is a moiety numbering 0 to 5 whichmay be the same or different and are independently selected from thegroup consisting of H; OH; NH₂;

where n is defined above and t=1 to 5; and R₂ is H or alkyl.
 2. Thecompound of claim 1, wherein M is H.
 3. The compound of claim 1, whereinAr¹ is 4-phenyl.
 4. The compound of claim 1, wherein Ar¹ is 4-pyridyl.5. The compound of claim 3, wherein said phenyl is substituted on thering with at least one of CN, OCF₃, F and Cl or combinations thereof. 6.The compound of claim 3, wherein said substituents are in position 3 onthe ring with respect to said ring's attachment to the benzylic positionin Formula I.
 7. The compound of claim 4, wherein said pyridyl issubstituted on the ring with at least one of CN, OCF₃, F and Cl orcombinations thereof.
 8. The compound of claim 1, wherein Z isAr²—NH—CO, where Ar² is phenyl.
 9. The compound of claim 8, wherein saidphenyl is substituted with one or more moieties which number 0 to 5, maybe the same or different and are independently selected from the groupconsisting of F, Cl, Br, I, OCH₃, and CF₃.
 10. The compound of claim 9,wherein said substituent on Ar² is F, Cl or OCH₃.
 11. The compound ofclaim 1, wherein R is a C₁-C₄ straight chain alkyl, a C₁-C₄ branchedalkyl or a C₃-C₇ cycloalkyl.
 12. The compound of claim 11, wherein R ismethyl, ethyl or propyl.
 13. The compound of claim 11, wherein R isisopropyl.
 14. The compound of claim 11, wherein R is cyclobutyl. 15.The compound of claim 1, wherein n is 2-4.
 16. The compound of claim 1,wherein n is
 2. 17. The compound of claim 1, wherein R₁ is selected fromthe group consisting of NH₂; NHR; N(R)₂; N(R)₂→O; NH(CH₂)_(n)OCH₃;N(R)SO₂R; NH(CH₂)_(n)—N(R)₂; N(R)SO₂(R);

with R and Y defined in claim
 1. 18. The compound of claim 17, whereinR₁ is selected from the group consisting of NHMe; NHEt; NMe₂;NH(CH₂)_(n)OCH₃; NH-cyclopropyl; NH-cyclobutyl; NH-cyclopentyl;NH(CH₂)₃NMe₂;


19. The compound of claim 1, wherein Y is selected from the groupconsisting of NH₂; NMe₂; NHMe;


20. A compound, including enantiomers, stereoisomers, rotamers,tautomers and prodrug of said compound, and pharmaceutically acceptablesalts or solvates of said compound or of said prodrug, said compoundhaving the general structure shown in Formula II:

wherein: M is H or R; k=0 to5; p=1 to 6; n=0 to 6; Z=

where Ar² is an unsubstituted or substituted phenyl with saidsubstituents numbering 0 to 5 which may be the same or different and areindependently selected from the group consisting of F, Cl, Br, I, R, OR,NO₂, and CF₃; R₁ may be the same or different and are independentlyselected from the group consisting of R; NH₂; NHR; N(R)₂; N(R)₂→O;NH(CH₂)_(n)OR; N(R)SO₂R; NH(CH₂)_(n)—N(R)₂; N(R)SO₂(R);

where n and R are defined above and Y is a moiety numbering 0 to 5 whichmay be the same or different and are independently selected from thegroup consisting of H; OH; NH₂;

where n is defined above and t=1 to 5; and X may be the same ordifferent, and are independently selected from the group consisting of:H, Cl, F, Br, I, R, OR, CF₃, OCF₃, methylenedioxy, phenyl,


21. The compound of claim 20, wherein k numbers 1-3.
 22. The compound ofclaim 20, wherein X is selected from the group consisting of R, H, Cl,CF₃ and OCF₃ where R is as defined in claim
 20. 23. The compound ofclaim 20 wherein M is H.
 24. The compound of claim 20, wherein Z isAr²—NH—CO, where Ar² is phenyl.
 25. The compound of claim 24, whereinsaid phenyl is substituted with one or more moieties which number 0 to5, may be the same or different and are independently selected from thegroup consisting of F, Cl, Br, I, OCH₃, and CF₃.
 26. The compound ofclaim 20, wherein R is a C₁-C₄ straight chain or branched alkyl.
 27. Thecompound of claim 20, wherein n is
 2. 28. A pharmaceutical compositioncomprising as an active ingredient at least one compound of claim 1 orclaim
 20. 29. The pharmaceutical composition of claim 28 for use intreating disorders associated with the MCH receptor.
 30. Thepharmaceutical composition of claim 28 additionally comprising apharmaceutically acceptable carrier.
 31. A method of treating disordersassociated with the MCH receptor, said method comprising administeringto a patient in need of such treatment a pharmaceutical compositionwhich composition comprises therapeutically effective amounts of atleast one compound of claim 1 or of claim
 20. 32. The method of claim31, wherein said administration is oral.
 33. The method of claim 31,wherein said administration is via subcutaneous administration.
 34. Theuse of a compound of claim 1 or claim 20 for the manufacture of amedicament to treat disorders associated with the MCH receptor.
 35. Amethod of preparing a pharmaceutical composition for treating disordersassociated with the MCH receptor, said method comprising bringing intointimate contact at least one compound of a compound of claim 1 or ofclaim 20 and a pharmaceutically acceptable carrier.
 36. A compoundexhibiting MCH modulatory activity, including enantiomers,stereoisomers, rotamers and tautomers of said compound, andpharmaceutically acceptable salts or solvates of said compound, saidcompound being selected from the group of compounds with structureslisted below:


37. A compound, including enantiomers, stereoisomers, rotamers,tautomers and prodrug of said compound, and pharmaceutically acceptablesalts or solvates of said compound or of said prodrug, said compoundhaving the general structure shown in Formula III:

wherein: M is H or R; k=0 to 5; p=1 to 6; n=0 to 6; G is a moietyselected from the group consisting of —CH₂—, —C(O)— and —C(O)—O— withthe —C(O) linked to the N(R₁R₂) in the figure; R₁ may be the same ordifferent and are independently selected from the group consisting of R;NH₂; NHR; N(R)₂; N(R)₂→O; NH(CH₂)_(n)OR; N(R)SO₂R; NH(CH₂)_(n)—N(R)₂;N(R)SO₂(R);

where n and R are defined above and Y is a moiety numbering 0 to 5 whichmay be the same or different and are independently selected from thegroup consisting of H; OH; NH₂;

where n is defined above and t=1 to 5; R₂ is H or alkyl; R₃ is selectedfrom the group consisting of alkyl, aryl, arylalkyl and alkylaryl; and Lmay be the same or different and is independently selected from thegroup consisting of H, aryl, alkyl, halogen, alkoxy, aryloxy,arylalkoxy, alkylaryloxy, hydroxy, carboxy, carboalkoxy, cyano, CF₃ andNO₂.
 38. A pharmaceutical composition for treating disorders associatedwith the MCH receptor, said composition comprising therapeuticallyeffective amounts of at least one compound of claim 36 and apharmaceutically acceptable carrier.
 39. A pharmaceutical composition totreat eating disorders said composition comprising: therapeuticallyeffective amounts of at least one compound of claim 1 or of claim 20, aprodrug thereof, or a pharmaceutically acceptable salt of said compoundor of said prodrug; therapeutically effective amounts of one or morecompounds, said compounds being selected from the group consisting of aβ₃ agonist, a thryomimetic agent, an antiobesity agent, an anorecticagent and an NPY antagonist; and a pharmaceutically acceptable carrier.40. A method of treating eating disorders which method comprisesadministering to a mammal in need of such treatment: (a) therapeuticallyeffective amounts of at least one compound of claim 1 or of claim 20, aprodrug thereof, or a pharmaceutically acceptable salt of said compoundor of said prodrug; and (b) therapeutically effective amounts of one ormore compounds, said compounds being selected from the group consistingof a β₃ agonist, a thryomimetic agent, an antiobesity agent, ananorectic agent and an NPY antagonist; wherein the amounts in (a) and(b) result in said treatment.
 41. A pharmaceutical composition to treateating disorders said composition comprising: therapeutically effectiveamounts of at least one compound of claim 1 or of claim 20, a prodrugthereof, or a pharmaceutically acceptable salt of said compound or ofsaid prodrug; therapeutically effective amounts of one or more compoundsselected from the group consisting of an analdose reductase inhibitor, aglycogen phosphorylase inhibitor, a sorbitol dehydrogenase inhibitor, aprotein tyrosine phosphatase 1B inhibitor, a dipeptidyl proteaseinhibitor, insulin, an insulin mimetic, metformin, acarbose, aPPAR-gamma ligand, rosaglitazone, pioglitazone, GW1929, a sulfonylurea,glipazide, glyburide, and chlorpropamide; and a pharmaceuticallyacceptable carrier.